geneid | 81619 |
---|---|
ensemblid | ENSG00000108219.16 |
hgncid | 23303 |
symbol | TSPAN14 |
name | tetraspanin 14 |
refseq_nuc | NM_030927.4 |
refseq_prot | NP_112189.2 |
ensembl_nuc | ENST00000429989.8 |
ensembl_prot | ENSP00000396270.2 |
mane_status | MANE Select |
chr | chr10 |
start | 80454310 |
end | 80522631 |
strand | + |
ver | v1.2 |
region | chr10:80454310-80522631 |
region5000 | chr10:80449310-80527631 |
regionname0 | TSPAN14_chr10_80454310_80522631 |
regionname5000 | TSPAN14_chr10_80449310_80527631 |
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 | 270 | 252 | 88 | 64 | 46 | 12 | 40 | 26 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
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 | 813 | 233 | 72 | 62 | 46 | 12 | 39 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
c0002 | 0/0 | 813 | 15 | 13 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
c0003 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
c0004 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
c0005 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4739 | 46 | 2 | 16 | 18 | 2 | 8 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0002 | 0/0 | 4739 | 33 | 18 | 6 | 1 | 1 | 7 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0003 | 0/1 | 4735 | 18 | 2 | 10 | 1 | 3 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0004 | 0/0 | 4741 | 16 | 0 | 1 | 12 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0005 | 0/0 | 4741 | 11 | 9 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0006 | 0/0 | 4739 | 10 | 6 | 2 | 0 | 0 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0007 | 0/0 | 4741 | 8 | 3 | 1 | 1 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0008 | 0/0 | 4740 | 8 | 1 | 4 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0009 | 0/0 | 4740 | 7 | 3 | 1 | 0 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0010 | 0/0 | 4739 | 6 | 0 | 4 | 0 | 1 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0011 | 0/0 | 4738 | 6 | 0 | 2 | 0 | 2 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0012 | 0/0 | 4740 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0013 | 0/0 | 4739 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0014 | 0/0 | 4740 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0015 | 0/0 | 4740 | 4 | 0 | 1 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0016 | 0/0 | 4739 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0017 | 0/0 | 4746 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0018 | 0/0 | 4739 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0019 | 0/0 | 4739 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0020 | 0/0 | 4739 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0021 | 0/0 | 4740 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0022 | 0/0 | 4740 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0023 | 0/0 | 4740 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0024 | 0/0 | 4739 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0025 | 0/0 | 4738 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0026 | 0/0 | 4738 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0027 | 0/0 | 4739 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0028 | 0/0 | 4738 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0029 | 0/0 | 4739 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0030 | 0/0 | 4739 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0031 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0032 | 0/0 | 4740 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0033 | 0/0 | 4739 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0034 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0035 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0036 | 0/0 | 4740 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0037 | 0/0 | 4740 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0038 | 0/0 | 4740 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0039 | 0/0 | 4741 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0040 | 0/0 | 4741 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0041 | 1/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0042 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0043 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0044 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0045 | 0/0 | 4740 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0046 | 0/0 | 4739 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0047 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0048 | 0/0 | 4739 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0049 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0050 | 0/0 | 4739 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0051 | 0/0 | 4740 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0052 | 0/0 | 4739 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0053 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0054 | 0/0 | 4742 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0055 | 0/0 | 4739 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0056 | 0/0 | 4739 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
t0057 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
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 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
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 | 813 | 233 | 72 | 62 | 46 | 12 | 39 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0002 | 0/0 | 813 | 15 | 13 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0003 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0004 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0005 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5551 | 46 | 2 | 16 | 18 | 2 | 8 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0002 | 0/0 | 5551 | 33 | 18 | 6 | 1 | 1 | 7 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0003 | 0/1 | 5547 | 18 | 2 | 10 | 1 | 3 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0004 | 0/0 | 5553 | 16 | 0 | 1 | 12 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0006 | 0/0 | 5551 | 9 | 5 | 2 | 0 | 0 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0007 | 0/0 | 5553 | 8 | 3 | 1 | 1 | 0 | 3 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0008 | 0/0 | 5552 | 8 | 1 | 4 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0009 | 0/0 | 5552 | 6 | 3 | 1 | 0 | 0 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0010 | 0/0 | 5551 | 6 | 0 | 4 | 0 | 1 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0011 | 0/0 | 5550 | 6 | 0 | 2 | 0 | 2 | 2 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0012 | 0/0 | 5552 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0013 | 0/0 | 5551 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0014 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0015 | 0/0 | 5552 | 4 | 0 | 1 | 2 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0016 | 0/0 | 5551 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0017 | 0/0 | 5558 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0018 | 0/0 | 5551 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0019 | 0/0 | 5551 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0020 | 0/0 | 5551 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0022 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0023 | 0/0 | 5552 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0024 | 0/0 | 5551 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0025 | 0/0 | 5550 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0026 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0027 | 0/0 | 5551 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0028 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0029 | 0/0 | 5551 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0030 | 0/0 | 5551 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0031 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0032 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0033 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0034 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0035 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0036 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0037 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0038 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0039 | 0/0 | 5553 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0040 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0041 | 1/0 | 5547 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0042 | 0/0 | 5547 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0043 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0044 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0045 | 0/0 | 5552 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0046 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0047 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0048 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0049 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0050 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0051 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0052 | 0/0 | 5551 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0053 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0055 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0056 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0001t0057 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0002t0005 | 0/0 | 5553 | 11 | 9 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0002t0021 | 0/0 | 5552 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0002t0054 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0003t0014 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0003t0018 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0004t0009 | 0/0 | 5552 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
a0001c0005t0006 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | copy fasta | chr10 | 80449310 | 80527631 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0007 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0010g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0011g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0011g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0013g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0015g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0015g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0015g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0015g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0016g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0017g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0018g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0020g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0020g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0020g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0022g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0022g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0022g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0024g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0024g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0025g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0025g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0026g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0026g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0027g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0027g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0028g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0028g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0029g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0029g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0030g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0031g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0032g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0033g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0034g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0035g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0036g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0037g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0038g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0039g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0040g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0041g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0042g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0043g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0044g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0045g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0046g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0047g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0048g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0049g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0050g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0051g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0052g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0053g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0055g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0056g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0001t0057g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0002t0054g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0003t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0003t0018g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0004t0009g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
a0001c0005t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0042 | g0050 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00140 | hp1 | a0001 | c0001 | t0025 | g0151 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0061 | EUR | GBR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | FIN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00438 | hp1 | a0001 | c0001 | t0015 | g0195 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00438 | hp2 | a0001 | c0001 | t0015 | g0049 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00558 | hp1 | a0001 | c0001 | t0028 | g0227 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00558 | hp2 | a0001 | c0001 | t0028 | g0162 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00639 | hp1 | a0001 | c0002 | t0005 | g0239 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00639 | hp2 | a0001 | c0001 | t0031 | g0143 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00642 | hp1 | a0001 | c0001 | t0046 | g0037 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0096 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0192 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00741 | hp1 | a0001 | c0001 | t0011 | g0135 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG00741 | hp2 | a0001 | c0001 | t0045 | g0038 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01069 | hp1 | a0001 | c0001 | t0043 | g0031 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01070 | hp2 | a0001 | c0001 | t0044 | g0047 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0048 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01074 | hp2 | a0001 | c0001 | t0029 | g0170 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01081 | hp1 | a0001 | c0001 | t0020 | g0152 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01081 | hp2 | a0001 | c0001 | t0012 | g0017 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0199 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01099 | hp2 | a0001 | c0001 | t0029 | g0178 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01109 | hp2 | a0001 | c0001 | t0020 | g0150 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0193 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01169 | hp2 | a0001 | c0001 | t0053 | g0137 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0145 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01243 | hp1 | a0001 | c0001 | t0033 | g0124 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01243 | hp2 | a0001 | c0001 | t0027 | g0093 | AMR | PUR | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01255 | hp2 | a0001 | c0001 | t0011 | g0006 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0149 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0068 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01433 | hp1 | a0001 | c0001 | t0013 | g0117 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01515 | hp1 | a0001 | c0001 | t0011 | g0078 | EUR | IBS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01884 | hp1 | a0001 | c0002 | t0021 | g0185 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01928 | hp1 | a0001 | c0001 | t0015 | g0010 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01975 | hp2 | a0001 | c0001 | t0010 | g0147 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01978 | hp1 | a0001 | c0001 | t0010 | g0144 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02015 | hp1 | a0001 | c0001 | t0055 | g0100 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0226 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02080 | hp1 | a0001 | c0001 | t0049 | g0159 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0002 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CDX | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02258 | hp1 | a0001 | c0001 | t0047 | g0214 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02258 | hp2 | a0001 | c0001 | t0050 | g0228 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0055 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02280 | hp2 | a0001 | c0002 | t0005 | g0238 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02451 | hp2 | a0001 | c0001 | t0024 | g0243 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0230 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0224 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02615 | hp2 | a0001 | c0001 | t0017 | g0056 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02622 | hp1 | a0001 | c0001 | t0048 | g0123 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02622 | hp2 | a0001 | c0001 | t0022 | g0244 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02630 | hp1 | a0001 | c0001 | t0023 | g0014 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02630 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0121 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0054 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02723 | hp2 | a0001 | c0005 | t0006 | g0134 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02735 | hp1 | a0001 | c0001 | t0034 | g0022 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02738 | hp1 | a0001 | c0001 | t0030 | g0148 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02738 | hp2 | a0001 | c0001 | t0032 | g0069 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02809 | hp1 | a0001 | c0003 | t0018 | g0125 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0131 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0001 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02896 | hp2 | a0001 | c0002 | t0005 | g0028 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02897 | hp2 | a0001 | c0001 | t0016 | g0001 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0240 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02965 | hp2 | a0001 | c0001 | t0057 | g0120 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02970 | hp2 | a0001 | c0001 | t0019 | g0216 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0090 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03017 | hp1 | a0001 | c0001 | t0052 | g0012 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03041 | hp2 | a0001 | c0003 | t0014 | g0122 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03098 | hp1 | a0001 | c0001 | t0019 | g0118 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0232 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03130 | hp1 | a0001 | c0001 | t0024 | g0112 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03139 | hp1 | a0001 | c0001 | t0017 | g0002 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0089 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03195 | hp1 | a0001 | c0001 | t0027 | g0094 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0186 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03225 | hp2 | a0001 | c0001 | t0022 | g0246 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0127 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0018 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03492 | hp1 | a0001 | c0001 | t0020 | g0119 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03516 | hp1 | a0001 | c0001 | t0040 | g0081 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03516 | hp2 | a0001 | c0002 | t0005 | g0059 | AFR | ESN | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03540 | hp1 | a0001 | c0002 | t0005 | g0024 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03540 | hp2 | a0001 | c0001 | t0016 | g0225 | AFR | GWD | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0215 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0163 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0101 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03704 | hp1 | a0001 | c0001 | t0038 | g0076 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03704 | hp2 | a0001 | c0001 | t0039 | g0130 | SAS | PJL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03831 | hp1 | a0001 | c0001 | t0009 | g0142 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03831 | hp2 | a0001 | c0004 | t0009 | g0098 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03927 | hp1 | a0001 | c0001 | t0011 | g0196 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03927 | hp2 | a0001 | c0001 | t0008 | g0133 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04115 | hp2 | a0001 | c0001 | t0051 | g0060 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0077 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04184 | hp2 | a0001 | c0001 | t0015 | g0208 | SAS | BEB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0079 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0073 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0107 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0070 | SAS | STU | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0111 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18522 | hp2 | a0001 | c0001 | t0022 | g0245 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18906 | hp2 | a0001 | c0001 | t0023 | g0015 | AFR | YRI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18942 | hp2 | a0001 | c0001 | t0036 | g0116 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18947 | hp1 | a0001 | c0001 | t0026 | g0161 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18953 | hp2 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0110 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18994 | hp1 | a0001 | c0001 | t0035 | g0223 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19030 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19030 | hp2 | a0001 | c0002 | t0054 | g0016 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19043 | hp2 | a0001 | c0002 | t0021 | g0184 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19063 | hp1 | a0001 | c0001 | t0026 | g0242 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19063 | hp2 | a0001 | c0001 | t0037 | g0104 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0241 | AFR | ASW | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ASW | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20752 | hp1 | a0001 | c0001 | t0011 | g0006 | EUR | TSI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20752 | hp2 | a0001 | c0001 | t0025 | g0190 | EUR | TSI | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | GIH | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02109 | hp1 | a0001 | c0001 | t0056 | g0139 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02486 | hp1 | a0001 | c0002 | t0021 | g0187 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
HG03471 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | MSL | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | USA | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
NA21309 | hp2 | a0001 | c0001 | t0014 | g0058 | AFR | LWK | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0007 | REF | REF | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0041 | g0042 | REF | REF | TSPAN14_chr10_80449310_80527631 | TSPAN14 | chr10 | 80449310 | 80527631 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:80489284
|
C | T | 1 | a0001c0003 | 2 | HG02809.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.51C>T | p.Tyr17Tyr | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/9 | 130/5547 | 51/813 | 17/270 | chr10 | 80489284 | ||
chr10:80509429
|
C | T | 1 | a0001c0005 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.408C>T | p.Asp136Asp | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/9 | 487/5547 | 408/813 | 136/270 | chr10 | 80509429 | ||
chr10:80516287
|
T | C | 1 | a0001c0002 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
synonymous_variant | LOW | c.705T>C | p.Ile235Ile | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/9 | 784/5547 | 705/813 | 235/270 | chr10 | 80516287 | ||
chr10:80516305
|
C | T | 1 | a0001c0004 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.723C>T | p.Ile241Ile | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/9 | 802/5547 | 723/813 | 241/270 | chr10 | 80516305 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:80518104
|
G | A | 1 | a0001c0001t0023 | 2 | HG02630.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 128 | chr10 | 80518104 | |||||
chr10:80518293
|
C | G | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*317C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 317 | chr10 | 80518293 | |||||
chr10:80518386
|
G | A | 1 | a0001c0001t0030 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 410 | chr10 | 80518386 | |||||
chr10:80518407
|
C | T | 1 | a0001c0001t0029 | 2 | HG01074.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*431C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 431 | chr10 | 80518407 | |||||
chr10:80518424
|
T | C | 3 | a0001c0001t0010a0001c0001t0031a0001c0001t0032 | 8 | HG00140.hp2 HG00639.hp2 HG01192.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 448 | chr10 | 80518424 | |||||
chr10:80518469
|
C | T | 1 | a0001c0001t0022 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*493C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 493 | chr10 | 80518469 | |||||
chr10:80518470
|
G | A | 4 | a0001c0001t0018a0001c0001t0024a0001c0001t0033others(1): Show | 6 | HG01243.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*494G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 494 | chr10 | 80518470 | |||||
chr10:80518704
|
C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 728 | chr10 | 80518704 | |||||
chr10:80519063
|
C | T | 1 | a0001c0001t0056 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1087C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1087 | chr10 | 80519063 | |||||
chr10:80519158
|
T | G | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1182T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1182 | chr10 | 80519158 | |||||
chr10:80519174
|
C | T | 1 | a0001c0001t0055 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1198 | chr10 | 80519174 | |||||
chr10:80519238
|
A | T | 3 | a0001c0002t0005a0001c0002t0021a0001c0002t0054 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1262A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1262 | chr10 | 80519238 | |||||
chr10:80519305
|
G | C | 1 | a0001c0001t0035 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1329 | chr10 | 80519305 | |||||
chr10:80519314
|
T | C | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0036others(4): Show | 29 | HG00597.hp2 HG01175.hp2 HG02004.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1338T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1338 | chr10 | 80519314 | |||||
chr10:80519343
|
G | T | 1 | a0001c0001t0053 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1367 | chr10 | 80519343 | |||||
chr10:80519362
|
G | T | 1 | a0001c0001t0052 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1386 | chr10 | 80519362 | |||||
chr10:80519446
|
C | G | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1470C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1470 | chr10 | 80519446 | |||||
chr10:80519514
|
A | ATTT | 6 | a0001c0001t0011a0001c0001t0013a0001c0001t0025others(3): Show | 15 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1551dupTTT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | ||||
chr10:80519514
|
A | ATTTT | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(29): Show | 145 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1548_*1551dupTTTT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | ||||
chr10:80519514
|
A | ATTTTT | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(11): Show | 51 | HG00597.hp2 HG00735.hp1 HG01081.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1547_*1551dupTTTT others(1): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | ||||
chr10:80519514
|
A | ATTTTTT | 4 | a0001c0001t0040a0001c0002t0005a0001c0002t0021others(1): Show | 16 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1546_*1551dupTTTT others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | ||||
chr10:80519514
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1541_*1551dupTTTT others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1552 | INFO_REALIGN_3_PRIME | chr10 | 80519514 | ||||
chr10:80519571
|
G | A | 1 | a0001c0001t0055 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1595 | chr10 | 80519571 | |||||
chr10:80519681
|
A | G | 1 | a0001c0001t0042 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1705A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1705 | chr10 | 80519681 | |||||
chr10:80519787
|
C | T | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1811C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1811 | chr10 | 80519787 | |||||
chr10:80519797
|
A | G | 1 | a0001c0001t0050 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1821 | chr10 | 80519797 | |||||
chr10:80519801
|
AT | A | 5 | a0001c0001t0026a0001c0001t0037a0001c0001t0044others(2): Show | 6 | HG01070.hp2 HG01169.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1839delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1839 | INFO_REALIGN_3_PRIME | chr10 | 80519801 | ||||
chr10:80519822
|
C | G | 1 | a0001c0001t0049 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1846 | chr10 | 80519822 | |||||
chr10:80519844
|
G | A | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1868 | chr10 | 80519844 | |||||
chr10:80519867
|
G | A | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1891G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1891 | chr10 | 80519867 | |||||
chr10:80519894
|
C | T | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1918C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 1918 | chr10 | 80519894 | |||||
chr10:80520059
|
T | C | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2083T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2083 | chr10 | 80520059 | |||||
chr10:80520171
|
C | T | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(13): Show | 90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2195C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2195 | chr10 | 80520171 | |||||
chr10:80520204
|
C | T | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(7): Show | 71 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2228 | chr10 | 80520204 | |||||
chr10:80520326
|
A | G | 1 | a0001c0001t0024 | 2 | HG02451.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2350A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2350 | chr10 | 80520326 | |||||
chr10:80520381
|
T | C | 1 | a0001c0001t0053 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2405T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2405 | chr10 | 80520381 | |||||
chr10:80520381
|
T | G | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(53): Show | 230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2405T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2405 | chr10 | 80520381 | |||||
chr10:80520384
|
C | T | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(13): Show | 90 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2408C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2408 | chr10 | 80520384 | |||||
chr10:80520432
|
A | G | 3 | a0001c0002t0005a0001c0002t0021a0001c0002t0054 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2456A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2456 | chr10 | 80520432 | |||||
chr10:80520543
|
C | G | 4 | a0001c0001t0013a0001c0001t0014a0001c0001t0048others(1): Show | 9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2567C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2567 | chr10 | 80520543 | |||||
chr10:80520608
|
A | G | 1 | a0001c0001t0027 | 2 | HG01243.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2632 | chr10 | 80520608 | |||||
chr10:80520631
|
G | A | 2 | a0001c0001t0045a0001c0001t0046 | 2 | HG00642.hp1 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2655G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2655 | chr10 | 80520631 | |||||
chr10:80520635
|
C | T | 1 | a0001c0001t0039 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2659C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2659 | chr10 | 80520635 | |||||
chr10:80520795
|
T | G | 3 | a0001c0002t0005a0001c0002t0021a0001c0002t0054 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2819T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2819 | chr10 | 80520795 | |||||
chr10:80520954
|
G | A | 1 | a0001c0001t0020 | 3 | HG01081.hp1 HG01109.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2978G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 2978 | chr10 | 80520954 | |||||
chr10:80521445
|
T | C | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3469T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3469 | chr10 | 80521445 | |||||
chr10:80521493
|
T | G | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0036others(4): Show | 29 | HG00597.hp2 HG01175.hp2 HG02004.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3517T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3517 | chr10 | 80521493 | |||||
chr10:80521684
|
T | C | 1 | a0001c0001t0017 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3708T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3708 | chr10 | 80521684 | |||||
chr10:80521851
|
G | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3875G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3875 | chr10 | 80521851 | |||||
chr10:80521852
|
A | T | 1 | a0001c0001t0033 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3876A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3876 | chr10 | 80521852 | |||||
chr10:80521872
|
C | T | 1 | a0001c0001t0057 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3896C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3896 | chr10 | 80521872 | |||||
chr10:80521911
|
G | GA | 14 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(11): Show | 51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3954dupA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3955 | INFO_REALIGN_3_PRIME | chr10 | 80521911 | ||||
chr10:80521911
|
GA | G | 7 | a0001c0001t0018a0001c0001t0024a0001c0001t0028others(4): Show | 12 | HG00558.hp1 HG00558.hp2 HG01243.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3954delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3954 | INFO_REALIGN_3_PRIME | chr10 | 80521911 | ||||
chr10:80521914
|
A | G | 1 | a0001c0001t0016 | 4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3938A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3938 | chr10 | 80521914 | |||||
chr10:80521958
|
C | T | 2 | a0001c0001t0012a0001c0001t0023 | 8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3982C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 3982 | chr10 | 80521958 | |||||
chr10:80522133
|
C | T | 3 | a0001c0002t0005a0001c0002t0021a0001c0002t0054 | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4157C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4157 | chr10 | 80522133 | |||||
chr10:80522222
|
T | C | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*4246T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4246 | chr10 | 80522222 | |||||
chr10:80522426
|
G | A | 1 | a0001c0001t0019 | 3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4450G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4450 | chr10 | 80522426 | |||||
chr10:80522502
|
C | A | 4 | a0001c0001t0004a0001c0001t0036a0001c0001t0037others(1): Show | 19 | HG00597.hp2 HG02004.hp2 HG02074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4526C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4526 | chr10 | 80522502 | |||||
chr10:80522560
|
A | G | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0016others(2): Show | 13 | HG01433.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4584A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 9/9 | 4584 | chr10 | 80522560 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:80454530
|
G | C | 1 | a0001c0001t0003g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18+159G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454530 | ||||||
chr10:80454561
|
C | A | 3 | a0001c0001t0001g0009a0001c0001t0004g0008a0001c0001t0015g0010 | 3 | HG01167.hp2 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-18+190C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454561 | ||||||
chr10:80454696
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+325C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454696 | ||||||
chr10:80454712
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0052g0012 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-18+341G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454712 | ||||||
chr10:80454715
|
G | T | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+344G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454715 | ||||||
chr10:80454745
|
G | A | 7 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(4): Show | 7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+374G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454745 | ||||||
chr10:80454758
|
C | G | 1 | a0001c0001t0024g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+387C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454758 | ||||||
chr10:80454766
|
C | T | 1 | a0001c0001t0026g0242 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-18+395C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454766 | ||||||
chr10:80454788
|
G | C | 1 | a0001c0001t0004g0021 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-18+417G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454788 | ||||||
chr10:80454830
|
A | C | 213 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0071others(210): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18+459A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454830 | ||||||
chr10:80454879
|
C | T | 6 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0002t0005g0238others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+508C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454879 | ||||||
chr10:80454941
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+570C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80454941 | ||||||
chr10:80455036
|
C | T | 168 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(165): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-18+665C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455036 | ||||||
chr10:80455065
|
G | A | 29 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(26): Show | 30 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+694G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455065 | ||||||
chr10:80455121
|
C | T | 13 | a0001c0001t0004g0021a0001c0001t0004g0099a0001c0001t0004g0102others(10): Show | 13 | HG02015.hp1 HG03654.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+750C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455121 | ||||||
chr10:80455207
|
C | G | 6 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+836C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455207 | ||||||
chr10:80455290
|
T | C | 1 | a0001c0001t0007g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+919T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455290 | ||||||
chr10:80455532
|
T | C | 174 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(171): Show | 178 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-18+1161T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455532 | ||||||
chr10:80455868
|
C | T | 1 | a0001c0001t0024g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+1497C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455868 | ||||||
chr10:80455890
|
C | T | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+1519C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80455890 | ||||||
chr10:80456046
|
C | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+1675C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456046 | ||||||
chr10:80456111
|
A | G | 28 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(25): Show | 29 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+1740A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456111 | ||||||
chr10:80456137
|
A | G | 1 | a0001c0001t0028g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+1766A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456137 | ||||||
chr10:80456402
|
A | G | 29 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(26): Show | 30 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18+2031A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456402 | ||||||
chr10:80456492
|
A | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+2121A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456492 | ||||||
chr10:80456552
|
A | G | 10 | a0001c0001t0002g0075a0001c0001t0007g0054a0001c0001t0007g0077others(7): Show | 10 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+2181A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456552 | ||||||
chr10:80456926
|
G | A | 124 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(121): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-18+2555G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80456926 | ||||||
chr10:80457271
|
C | T | 6 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0002t0005g0238others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+2900C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457271 | ||||||
chr10:80457371
|
T | G | 1 | a0001c0001t0024g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3000T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457371 | ||||||
chr10:80457405
|
T | C | 29 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(26): Show | 29 | HG01081.hp2 HG01175.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+3034T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457405 | ||||||
chr10:80457435
|
C | T | 5 | a0001c0001t0002g0074a0001c0001t0009g0073a0001c0001t0012g0018others(2): Show | 5 | HG02698.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+3064C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457435 | ||||||
chr10:80457656
|
C | G | 1 | a0001c0001t0008g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-18+3285C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457656 | ||||||
chr10:80457673
|
G | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+3302G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457673 | ||||||
chr10:80457792
|
C | T | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+3421C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457792 | ||||||
chr10:80457874
|
A | G | 1 | a0001c0001t0024g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+3503A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457874 | ||||||
chr10:80457953
|
G | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+3582G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457953 | ||||||
chr10:80457983
|
T | C | 7 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(4): Show | 7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+3612T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80457983 | ||||||
chr10:80458011
|
T | C | 6 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0016g0001others(3): Show | 8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+3640T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458011 | ||||||
chr10:80458118
|
C | T | 10 | a0001c0001t0002g0075a0001c0001t0007g0054a0001c0001t0007g0077others(7): Show | 10 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3747C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458118 | ||||||
chr10:80458188
|
G | A | 6 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3817G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458188 | ||||||
chr10:80458214
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0035g0223 | 3 | HG01978.hp2 HG02293.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-18+3843A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458214 | ||||||
chr10:80458238
|
GAGGTGAC others(3): Show |
G | 138 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(135): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+3873_-18+3882d others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80458238 | |||||
chr10:80458343
|
A | G | 6 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0002t0005g0238others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+3972A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458343 | ||||||
chr10:80458350
|
G | A | 1 | a0001c0001t0004g0099 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-18+3979G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458350 | ||||||
chr10:80458350
|
G | C | 151 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-18+3979G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458350 | ||||||
chr10:80458399
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18+4028C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458399 | ||||||
chr10:80458629
|
G | T | 19 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0003others(16): Show | 21 | HG00140.hp2 HG01123.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+4258G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458629 | ||||||
chr10:80458723
|
G | C | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-18+4352G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458723 | ||||||
chr10:80458766
|
G | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4395G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458766 | ||||||
chr10:80458882
|
C | T | 1 | a0001c0001t0028g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-18+4511C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458882 | ||||||
chr10:80458903
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0014g0055a0001c0001t0014g0058others(4): Show | 9 | HG01081.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+4532C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458903 | ||||||
chr10:80458916
|
A | G | 5 | a0001c0001t0003g0051a0001c0001t0003g0052a0001c0001t0003g0053others(2): Show | 5 | HG00099.hp1 HG00438.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+4545A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80458916 | ||||||
chr10:80458967
|
AT | A | 19 | a0001c0001t0002g0075a0001c0001t0003g0023a0001c0001t0006g0113others(16): Show | 19 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+4610delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80458967 | |||||
chr10:80459142
|
A | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4771A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459142 | ||||||
chr10:80459208
|
T | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(135): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-18+4837T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459208 | ||||||
chr10:80459310
|
T | C | 144 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(141): Show | 147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-18+4939T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459310 | ||||||
chr10:80459335
|
C | T | 5 | a0001c0001t0006g0048a0001c0001t0022g0244a0001c0001t0022g0245others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+4964C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459335 | ||||||
chr10:80459353
|
A | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+4982A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459353 | ||||||
chr10:80459466
|
G | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+5095G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459466 | ||||||
chr10:80459501
|
G | GT | 6 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0016g0001others(3): Show | 8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5131dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80459501 | |||||
chr10:80459577
|
C | G | 18 | a0001c0001t0002g0075a0001c0001t0006g0113a0001c0001t0006g0114others(15): Show | 18 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+5206C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459577 | ||||||
chr10:80459698
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-18+5327C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459698 | ||||||
chr10:80459730
|
C | T | 6 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+5359C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459730 | ||||||
chr10:80459783
|
G | A | 6 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0016g0001others(3): Show | 8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+5412G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459783 | ||||||
chr10:80459836
|
C | T | 6 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+5465C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459836 | ||||||
chr10:80459928
|
T | C | 1 | a0001c0001t0016g0001 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18+5557T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80459928 | ||||||
chr10:80460055
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-18+5684A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460055 | ||||||
chr10:80460102
|
T | C | 1 | a0001c0001t0051g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-18+5731T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460102 | ||||||
chr10:80460115
|
G | A | 2 | a0001c0002t0005g0024a0001c0002t0005g0025 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+5744G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460115 | ||||||
chr10:80460272
|
G | T | 1 | a0001c0001t0007g0110 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18+5901G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460272 | ||||||
chr10:80460503
|
G | A | 2 | a0001c0001t0004g0115a0001c0001t0036g0116 | 2 | NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-18+6132G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460503 | ||||||
chr10:80460534
|
C | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18942.hp1 NA18952.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-18+6163C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460534 | ||||||
chr10:80460644
|
C | G | 1 | a0001c0001t0019g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+6273C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460644 | ||||||
chr10:80460722
|
T | C | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+6351T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460722 | ||||||
chr10:80460758
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0153others(117): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.-18+6387C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460758 | ||||||
chr10:80460761
|
G | C | 1 | a0001c0001t0024g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18+6390G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460761 | ||||||
chr10:80460841
|
C | T | 213 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0071others(210): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-18+6470C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460841 | ||||||
chr10:80460947
|
G | A | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-18+6576G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460947 | ||||||
chr10:80460960
|
G | A | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+6589G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80460960 | ||||||
chr10:80461099
|
T | G | 13 | a0001c0001t0004g0021a0001c0001t0004g0099a0001c0001t0004g0102others(10): Show | 13 | HG02015.hp1 HG03654.hp1 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+6728T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461099 | ||||||
chr10:80461146
|
C | G | 11 | a0001c0001t0002g0075a0001c0001t0007g0054a0001c0001t0007g0077others(8): Show | 11 | HG01175.hp2 HG01515.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+6775C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461146 | ||||||
chr10:80461495
|
C | A | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+7124C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461495 | ||||||
chr10:80461634
|
T | C | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+7263T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461634 | ||||||
chr10:80461760
|
G | A | 2 | a0001c0001t0002g0229a0001c0002t0005g0230 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-18+7389G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461760 | ||||||
chr10:80461880
|
G | T | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+7509G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461880 | ||||||
chr10:80461915
|
CT | C | 16 | a0001c0001t0002g0075a0001c0001t0007g0054a0001c0001t0007g0077others(13): Show | 16 | HG01175.hp2 HG01433.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+7556delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80461915 | |||||
chr10:80461915
|
CTT | C | 13 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(10): Show | 15 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+7555_-18+7556d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80461915 | |||||
chr10:80461967
|
G | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+7596G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80461967 | ||||||
chr10:80462146
|
C | T | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+7775C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462146 | ||||||
chr10:80462163
|
T | C | 3 | a0001c0001t0023g0014a0001c0001t0023g0015a0001c0002t0054g0016 | 3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-18+7792T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462163 | ||||||
chr10:80462198
|
G | A | 1 | a0001c0001t0020g0119 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-18+7827G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462198 | ||||||
chr10:80462341
|
C | G | 32 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(29): Show | 34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+7970C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462341 | ||||||
chr10:80462347
|
A | AATGGGGT others(13): Show |
19 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(16): Show | 21 | HG00639.hp1 HG01074.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+7986_-18+7987i others(22): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80462347 | |||||
chr10:80462358
|
A | ATGGGATG others(13): Show |
3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+7992_-18+8011d others(22): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80462358 | |||||
chr10:80462358
|
A | G | 33 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(30): Show | 35 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18+7987A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462358 | ||||||
chr10:80462422
|
C | A | 223 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(220): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-18+8051C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462422 | ||||||
chr10:80462609
|
G | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+8238G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462609 | ||||||
chr10:80462942
|
T | C | 215 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(212): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-18+8571T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80462942 | ||||||
chr10:80463179
|
T | A | 32 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(29): Show | 34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+8808T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463179 | ||||||
chr10:80463183
|
G | A | 5 | a0001c0001t0013g0117a0001c0001t0018g0121a0001c0001t0019g0118others(2): Show | 5 | HG01433.hp1 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+8812G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463183 | ||||||
chr10:80463402
|
G | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(81): Show | 84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-18+9031G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463402 | ||||||
chr10:80463436
|
G | T | 1 | a0001c0001t0019g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+9065G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463436 | ||||||
chr10:80463535
|
C | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+9164C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463535 | ||||||
chr10:80463698
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-18+9327G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463698 | ||||||
chr10:80463731
|
G | A | 2 | a0001c0001t0013g0117a0001c0001t0019g0118 | 2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+9360G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80463731 | ||||||
chr10:80464011
|
A | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+9640A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464011 | ||||||
chr10:80464045
|
G | A | 1 | a0001c0001t0010g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18+9674G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464045 | ||||||
chr10:80464085
|
C | A | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-18+9714C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464085 | ||||||
chr10:80464183
|
C | T | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+9812C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464183 | ||||||
chr10:80464540
|
G | A | 32 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(29): Show | 34 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18+10169G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464540 | ||||||
chr10:80464648
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-18+10277C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464648 | ||||||
chr10:80464883
|
A | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+10512A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80464883 | ||||||
chr10:80465129
|
G | A | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+10758G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465129 | ||||||
chr10:80465141
|
G | A | 1 | a0001c0001t0008g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-18+10770G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465141 | ||||||
chr10:80465181
|
G | A | 4 | a0001c0001t0020g0119a0001c0001t0020g0150a0001c0001t0020g0152others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+10810G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465181 | ||||||
chr10:80465239
|
A | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+10868A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465239 | ||||||
chr10:80465245
|
C | A | 6 | a0001c0001t0007g0054a0001c0001t0007g0077a0001c0001t0007g0079others(3): Show | 6 | HG01175.hp2 HG01515.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+10874C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465245 | ||||||
chr10:80465403
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18+11032C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465403 | ||||||
chr10:80465619
|
C | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11248C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465619 | ||||||
chr10:80465620
|
C | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11249C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465620 | ||||||
chr10:80465681
|
A | T | 2 | a0001c0001t0006g0048a0001c0001t0044g0047 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18+11310A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465681 | ||||||
chr10:80465705
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+11334T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465705 | ||||||
chr10:80465807
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0052g0012 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-18+11436G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465807 | ||||||
chr10:80465854
|
C | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11483C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465854 | ||||||
chr10:80465891
|
C | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+11520C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80465891 | ||||||
chr10:80466006
|
AG | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+11637delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80466006 | |||||
chr10:80466037
|
T | C | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+11666T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466037 | ||||||
chr10:80466400
|
C | T | 1 | a0001c0001t0007g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+12029C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466400 | ||||||
chr10:80466483
|
T | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+12112T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466483 | ||||||
chr10:80466509
|
C | T | 31 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(28): Show | 32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+12138C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466509 | ||||||
chr10:80466619
|
A | C | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-18+12248A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466619 | ||||||
chr10:80466698
|
T | C | 23 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(20): Show | 25 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18+12327T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466698 | ||||||
chr10:80466795
|
C | T | 7 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+12424C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80466795 | ||||||
chr10:80467110
|
A | T | 16 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0099others(13): Show | 16 | HG02004.hp2 HG03654.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18+12739A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467110 | ||||||
chr10:80467156
|
A | G | 31 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(28): Show | 32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+12785A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467156 | ||||||
chr10:80467224
|
A | G | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+12853A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467224 | ||||||
chr10:80467347
|
C | T | 29 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(26): Show | 31 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+12976C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467347 | ||||||
chr10:80467387
|
A | G | 29 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(26): Show | 31 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18+13016A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467387 | ||||||
chr10:80467439
|
C | T | 1 | a0001c0003t0018g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+13068C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467439 | ||||||
chr10:80467447
|
G | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13076G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467447 | ||||||
chr10:80467468
|
C | T | 1 | a0001c0001t0019g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+13097C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467468 | ||||||
chr10:80467684
|
T | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+13313T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467684 | ||||||
chr10:80467739
|
C | G | 31 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(28): Show | 32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+13368C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467739 | ||||||
chr10:80467750
|
C | T | 1 | a0001c0001t0017g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18+13379C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467750 | ||||||
chr10:80467791
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+13420C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467791 | ||||||
chr10:80467791
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-18+13420C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467791 | ||||||
chr10:80467832
|
C | G | 1 | a0001c0001t0019g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+13461C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467832 | ||||||
chr10:80467874
|
T | A | 118 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(115): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-18+13503T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80467874 | ||||||
chr10:80467880
|
TTA | T | 3 | a0001c0001t0017g0002a0001c0001t0017g0056a0001c0001t0017g0057 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13511_-18+1351 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80467880 | |||||
chr10:80468241
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+13870A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468241 | ||||||
chr10:80468243
|
T | C | 2 | a0001c0001t0003g0034a0001c0001t0006g0035 | 2 | HG01257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-18+13872T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468243 | ||||||
chr10:80468258
|
C | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+13887C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468258 | ||||||
chr10:80468373
|
G | T | 5 | a0001c0001t0013g0117a0001c0001t0018g0121a0001c0001t0019g0118others(2): Show | 5 | HG01433.hp1 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+14002G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468373 | ||||||
chr10:80468431
|
A | G | 4 | a0001c0001t0002g0229a0001c0001t0002g0233a0001c0001t0002g0234others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+14060A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468431 | ||||||
chr10:80468536
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+14165C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468536 | ||||||
chr10:80468548
|
G | A | 6 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0016g0001others(3): Show | 8 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+14177G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468548 | ||||||
chr10:80468624
|
C | T | 1 | a0001c0001t0030g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+14253C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468624 | ||||||
chr10:80468715
|
TA | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+14347delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468715 | |||||
chr10:80468718
|
A | AT | 107 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(104): Show | 108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+14366dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468718 | |||||
chr10:80468718
|
AT | A | 24 | a0001c0001t0002g0005a0001c0001t0002g0062a0001c0001t0002g0074others(21): Show | 25 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18+14366delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80468718 | |||||
chr10:80468824
|
T | G | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+14453T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468824 | ||||||
chr10:80468942
|
A | G | 1 | a0001c0003t0018g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+14571A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80468942 | ||||||
chr10:80469205
|
C | T | 31 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(28): Show | 32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+14834C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469205 | ||||||
chr10:80469347
|
GATAA | G | 31 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(28): Show | 32 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-18+14984_-18+1498 others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80469347 | |||||
chr10:80469512
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+15141G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469512 | ||||||
chr10:80469524
|
C | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18+15153C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469524 | ||||||
chr10:80469550
|
C | T | 7 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+15179C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469550 | ||||||
chr10:80469673
|
T | G | 16 | a0001c0001t0001g0027a0001c0001t0001g0153a0001c0001t0001g0157others(13): Show | 16 | HG00558.hp2 HG00597.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18+15302T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469673 | ||||||
chr10:80469853
|
A | C | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15482A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469853 | ||||||
chr10:80469878
|
T | G | 1 | a0001c0001t0001g0217 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-18+15507T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80469878 | ||||||
chr10:80470000
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+15629C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470000 | ||||||
chr10:80470155
|
A | T | 31 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(28): Show | 33 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-18+15784A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470155 | ||||||
chr10:80470234
|
C | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+15863C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470234 | ||||||
chr10:80470390
|
C | T | 215 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(212): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-18+16019C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470390 | ||||||
chr10:80470398
|
C | G | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+16027C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470398 | ||||||
chr10:80470541
|
T | G | 2 | a0001c0001t0007g0054a0001c0001t0007g0077 | 2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+16170T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470541 | ||||||
chr10:80470895
|
G | A | 7 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+16524G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470895 | ||||||
chr10:80470918
|
G | A | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+16547G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470918 | ||||||
chr10:80470933
|
G | A | 2 | a0001c0001t0018g0121a0001c0001t0057g0120 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-18+16562G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470933 | ||||||
chr10:80470973
|
C | T | 1 | a0001c0002t0005g0096 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+16602C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80470973 | ||||||
chr10:80471007
|
C | T | 1 | a0001c0001t0004g0008 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-18+16636C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471007 | ||||||
chr10:80471175
|
G | T | 7 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+16804G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471175 | ||||||
chr10:80471329
|
GT | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0063a0001c0001t0002g0064 | 4 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+16961delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80471329 | |||||
chr10:80471584
|
A | G | 1 | a0001c0001t0033g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18+17213A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471584 | ||||||
chr10:80471783
|
G | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+17412G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471783 | ||||||
chr10:80471854
|
A | G | 1 | a0001c0001t0038g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-17363A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471854 | ||||||
chr10:80471992
|
T | C | 21 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(18): Show | 22 | HG00639.hp2 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-17225T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80471992 | ||||||
chr10:80472044
|
A | G | 1 | a0001c0001t0028g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-17-17173A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472044 | ||||||
chr10:80472062
|
C | G | 7 | a0001c0001t0016g0224a0001c0001t0016g0225a0001c0001t0018g0131others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-17155C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472062 | ||||||
chr10:80472095
|
G | A | 113 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-17-17122G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472095 | ||||||
chr10:80472203
|
G | T | 7 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-17014G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472203 | ||||||
chr10:80472292
|
G | T | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-16925G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472292 | ||||||
chr10:80472340
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-16877C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472340 | ||||||
chr10:80472404
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-16813G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472404 | ||||||
chr10:80472410
|
A | G | 7 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(4): Show | 7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-16807A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472410 | ||||||
chr10:80472413
|
G | A | 1 | a0001c0001t0002g0004 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-17-16804G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472413 | ||||||
chr10:80472422
|
C | T | 1 | a0001c0001t0035g0223 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-17-16795C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472422 | ||||||
chr10:80472509
|
G | A | 6 | a0001c0001t0016g0224a0001c0001t0016g0225a0001c0001t0033g0124others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-16708G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472509 | ||||||
chr10:80472681
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-16536T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472681 | ||||||
chr10:80472823
|
C | G | 1 | a0001c0002t0005g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-16394C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472823 | ||||||
chr10:80472859
|
T | G | 16 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0099others(13): Show | 16 | HG02004.hp2 HG03654.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-16358T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472859 | ||||||
chr10:80472885
|
T | C | 4 | a0001c0001t0033g0124a0001c0001t0048g0123a0001c0003t0014g0122others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-16332T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472885 | ||||||
chr10:80472950
|
G | A | 83 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0072others(80): Show | 86 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-17-16267G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80472950 | ||||||
chr10:80473000
|
T | C | 8 | a0001c0001t0002g0229a0001c0001t0012g0017a0001c0001t0012g0018others(5): Show | 8 | HG01081.hp2 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-16217T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473000 | ||||||
chr10:80473412
|
C | G | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-15805C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473412 | ||||||
chr10:80473433
|
G | C | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-15784G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473433 | ||||||
chr10:80473469
|
C | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-17-15748C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473469 | ||||||
chr10:80473517
|
T | C | 20 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0099others(17): Show | 20 | HG01243.hp1 HG02004.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-15700T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473517 | ||||||
chr10:80473599
|
C | G | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-15618C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473599 | ||||||
chr10:80473604
|
G | A | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-15613G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473604 | ||||||
chr10:80473609
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-17-15608G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473609 | ||||||
chr10:80473615
|
G | T | 4 | a0001c0001t0010g0061a0001c0001t0010g0068a0001c0001t0010g0127others(1): Show | 4 | HG00140.hp2 HG01358.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15602G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473615 | ||||||
chr10:80473628
|
C | T | 7 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(4): Show | 7 | HG01081.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-15589C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473628 | ||||||
chr10:80473659
|
G | C | 1 | a0001c0001t0057g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-15558G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473659 | ||||||
chr10:80473681
|
A | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-15536A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473681 | ||||||
chr10:80473682
|
TG | T | 4 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(1): Show | 4 | HG01081.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-15532delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473682 | |||||
chr10:80473684
|
GGT | G | 3 | a0001c0001t0023g0014a0001c0001t0023g0015a0001c0002t0054g0016 | 3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-15532_-17-1553 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473684 | ||||||
chr10:80473685
|
G | GT | 8 | a0001c0001t0001g0153a0001c0001t0004g0008a0001c0001t0004g0182others(5): Show | 8 | HG00558.hp2 HG02004.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-15516dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473685 | |||||
chr10:80473701
|
TA | T | 40 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(37): Show | 42 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-17-15513delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80473701 | |||||
chr10:80473702
|
A | T | 175 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(172): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-17-15515A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473702 | ||||||
chr10:80473703
|
A | T | 2 | a0001c0001t0001g0153a0001c0001t0028g0162 | 2 | HG00558.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-17-15514A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473703 | ||||||
chr10:80473727
|
T | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-15490T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473727 | ||||||
chr10:80473729
|
G | C | 5 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-15488G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473729 | ||||||
chr10:80473751
|
G | A | 10 | a0001c0001t0002g0183a0001c0001t0009g0186a0001c0001t0012g0188others(7): Show | 10 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-15466G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473751 | ||||||
chr10:80473784
|
G | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-17-15433G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473784 | ||||||
chr10:80473786
|
C | G | 27 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(24): Show | 29 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-17-15431C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473786 | ||||||
chr10:80473798
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-17-15419C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473798 | ||||||
chr10:80473863
|
C | T | 1 | a0001c0001t0008g0180 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-17-15354C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80473863 | ||||||
chr10:80474135
|
C | T | 1 | a0001c0001t0013g0117 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-17-15082C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474135 | ||||||
chr10:80474171
|
A | G | 6 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0233others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-15046A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474171 | ||||||
chr10:80474286
|
C | A | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14931C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474286 | ||||||
chr10:80474724
|
C | T | 30 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0231others(27): Show | 32 | HG00639.hp1 HG01074.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-17-14493C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474724 | ||||||
chr10:80474813
|
C | T | 1 | a0001c0001t0026g0161 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-17-14404C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474813 | ||||||
chr10:80474831
|
T | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0075a0001c0001t0002g0085others(83): Show | 89 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-14386T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474831 | ||||||
chr10:80474861
|
C | A | 26 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(23): Show | 28 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-14356C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474861 | ||||||
chr10:80474999
|
A | T | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14218A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80474999 | ||||||
chr10:80475021
|
G | A | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-14196G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475021 | ||||||
chr10:80475170
|
C | T | 16 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-14047C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475170 | ||||||
chr10:80475251
|
G | C | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-13966G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475251 | ||||||
chr10:80475383
|
T | C | 2 | a0001c0001t0022g0244a0001c0001t0022g0245 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-13834T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475383 | ||||||
chr10:80475531
|
T | A | 1 | a0001c0001t0022g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-13686T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475531 | ||||||
chr10:80475618
|
C | T | 18 | a0001c0001t0002g0075a0001c0001t0002g0229a0001c0001t0002g0233others(15): Show | 18 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-13599C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475618 | ||||||
chr10:80475640
|
T | C | 4 | a0001c0001t0016g0224a0001c0001t0016g0225a0001c0002t0005g0059others(1): Show | 4 | HG00642.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-13577T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475640 | ||||||
chr10:80475683
|
G | A | 6 | a0001c0001t0014g0058a0001c0001t0016g0001a0001c0001t0017g0002others(3): Show | 8 | HG01243.hp1 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-13534G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475683 | ||||||
chr10:80475742
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-17-13475A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475742 | ||||||
chr10:80475855
|
G | A | 22 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(19): Show | 23 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-13362G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475855 | ||||||
chr10:80475871
|
C | T | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-13346C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475871 | ||||||
chr10:80475881
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-13336G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80475881 | ||||||
chr10:80476009
|
G | A | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-13208G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476009 | ||||||
chr10:80476100
|
G | A | 1 | a0001c0001t0057g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-13117G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476100 | ||||||
chr10:80476110
|
G | A | 1 | a0001c0001t0014g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-13107G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476110 | ||||||
chr10:80476145
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-17-13072G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476145 | ||||||
chr10:80476169
|
C | T | 3 | a0001c0001t0023g0014a0001c0001t0023g0015a0001c0002t0054g0016 | 3 | HG02630.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-17-13048C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476169 | ||||||
chr10:80476173
|
T | C | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-13044T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476173 | ||||||
chr10:80476327
|
G | A | 28 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(25): Show | 28 | HG00642.hp2 HG01081.hp2 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.-17-12890G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476327 | ||||||
chr10:80476409
|
G | GT | 17 | a0001c0001t0002g0141a0001c0001t0003g0045a0001c0001t0003g0051others(14): Show | 17 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-12784dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GT | G | 71 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0071others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-17-12784delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTT | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0165a0001c0001t0002g0005others(14): Show | 18 | HG00741.hp2 HG01167.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-12785_-17-1278 others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTTT | G | 40 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0030others(37): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-17-12786_-17-1278 others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTTTT | G | 12 | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0183others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-12787_-17-1278 others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTTTTT | G | 6 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0004g0102others(3): Show | 6 | HG01074.hp1 HG02622.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-12788_-17-1278 others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTTTTTT | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-12789_-17-1278 others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476409
|
GTTTTTTT | G | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12790_-17-1278 others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80476409 | |||||
chr10:80476417
|
T | G | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-12800T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476417 | ||||||
chr10:80476418
|
T | G | 1 | a0001c0001t0004g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-17-12799T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476418 | ||||||
chr10:80476419
|
T | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-12798T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476419 | ||||||
chr10:80476420
|
T | G | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12797T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476420 | ||||||
chr10:80476439
|
G | A | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-12778G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476439 | ||||||
chr10:80476525
|
C | T | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-12692C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476525 | ||||||
chr10:80476625
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-12592C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476625 | ||||||
chr10:80476636
|
C | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-12581C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476636 | ||||||
chr10:80476743
|
T | G | 34 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(31): Show | 36 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-12474T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476743 | ||||||
chr10:80476860
|
G | A | 1 | a0001c0001t0016g0001 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-12357G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80476860 | ||||||
chr10:80477011
|
T | C | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-12206T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477011 | ||||||
chr10:80477086
|
G | A | 3 | a0001c0001t0009g0186a0001c0002t0021g0184a0001c0002t0021g0185 | 3 | HG01884.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17-12131G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477086 | ||||||
chr10:80477222
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(8): Show | 12 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-11995C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477222 | ||||||
chr10:80477370
|
A | G | 52 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0153others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-11847A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477370 | ||||||
chr10:80477592
|
G | A | 46 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(43): Show | 49 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-17-11625G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477592 | ||||||
chr10:80477625
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-11592T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80477625 | ||||||
chr10:80478009
|
A | G | 4 | a0001c0001t0012g0188a0001c0001t0023g0014a0001c0001t0023g0015others(1): Show | 4 | HG02559.hp1 HG02630.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-11208A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478009 | ||||||
chr10:80478139
|
A | G | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-11078A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478139 | ||||||
chr10:80478165
|
T | C | 1 | a0001c0001t0011g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-11052T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478165 | ||||||
chr10:80478232
|
T | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-10985T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478232 | ||||||
chr10:80478408
|
G | A | 1 | a0001c0001t0031g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17-10809G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478408 | ||||||
chr10:80478625
|
A | C | 1 | a0001c0001t0012g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-17-10592A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478625 | ||||||
chr10:80478641
|
G | A | 5 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0115others(2): Show | 5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-10576G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478641 | ||||||
chr10:80478647
|
C | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-17-10570C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478647 | ||||||
chr10:80478650
|
A | G | 1 | a0001c0001t0043g0031 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-17-10567A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478650 | ||||||
chr10:80478767
|
A | G | 1 | a0001c0001t0016g0001 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-10450A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478767 | ||||||
chr10:80478986
|
A | G | 10 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-10231A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80478986 | ||||||
chr10:80479080
|
T | G | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-10137T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479080 | ||||||
chr10:80479118
|
G | T | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-10099G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479118 | ||||||
chr10:80479162
|
G | GT | 5 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0048g0123others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-10052dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80479162 | |||||
chr10:80479274
|
T | C | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-9943T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479274 | ||||||
chr10:80479325
|
T | C | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-9892T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479325 | ||||||
chr10:80479372
|
C | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-9845C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479372 | ||||||
chr10:80479553
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-9664C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479553 | ||||||
chr10:80479640
|
C | G | 2 | a0001c0002t0005g0059a0001c0002t0005g0096 | 2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-9577C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479640 | ||||||
chr10:80479646
|
G | A | 3 | a0001c0001t0018g0121a0001c0001t0033g0124a0001c0001t0057g0120 | 3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-9571G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479646 | ||||||
chr10:80479763
|
C | G | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-9454C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479763 | ||||||
chr10:80479769
|
G | A | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-9448G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479769 | ||||||
chr10:80479773
|
C | T | 1 | a0001c0001t0055g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-17-9444C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479773 | ||||||
chr10:80479797
|
G | A | 101 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(98): Show | 106 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.-17-9420G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479797 | ||||||
chr10:80479900
|
T | C | 4 | a0001c0001t0003g0189a0001c0001t0025g0190a0001c0001t0045g0038others(1): Show | 4 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-9317T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479900 | ||||||
chr10:80479920
|
C | T | 4 | a0001c0002t0005g0238a0001c0002t0005g0239a0001c0002t0005g0240others(1): Show | 4 | HG00639.hp1 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9297C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479920 | ||||||
chr10:80479967
|
A | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-9250A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80479967 | ||||||
chr10:80480040
|
C | A | 237 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-17-9177C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480040 | ||||||
chr10:80480058
|
G | T | 1 | a0001c0001t0011g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-9159G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480058 | ||||||
chr10:80480096
|
T | C | 1 | a0001c0001t0030g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-17-9121T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480096 | ||||||
chr10:80480106
|
G | C | 4 | a0001c0001t0010g0061a0001c0001t0010g0068a0001c0001t0010g0127others(1): Show | 4 | HG00140.hp2 HG01358.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-9111G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480106 | ||||||
chr10:80480186
|
C | A | 100 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(97): Show | 105 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.-17-9031C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480186 | ||||||
chr10:80480202
|
A | G | 1 | a0001c0001t0004g0109 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-17-9015A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480202 | ||||||
chr10:80480445
|
T | A | 20 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0004g0008others(17): Show | 20 | HG01074.hp1 HG02004.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17-8772T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480445 | ||||||
chr10:80480480
|
C | T | 5 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0048g0123others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-8737C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480480 | ||||||
chr10:80480520
|
G | A | 2 | a0001c0001t0018g0121a0001c0001t0057g0120 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-8697G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480520 | ||||||
chr10:80480543
|
G | A | 104 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(101): Show | 109 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.-17-8674G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480543 | ||||||
chr10:80480572
|
C | T | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-8645C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480572 | ||||||
chr10:80480582
|
A | G | 1 | a0001c0001t0002g0004 | 2 | HG01123.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-17-8635A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480582 | ||||||
chr10:80480653
|
C | A | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-8564C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480653 | ||||||
chr10:80480673
|
C | T | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-8544C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480673 | ||||||
chr10:80480697
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-8520G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480697 | ||||||
chr10:80480814
|
A | T | 1 | a0001c0001t0003g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-17-8403A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480814 | ||||||
chr10:80480955
|
A | C | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-8262A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80480955 | ||||||
chr10:80481004
|
C | G | 84 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(81): Show | 84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-8213C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481004 | ||||||
chr10:80481186
|
G | A | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-8031G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481186 | ||||||
chr10:80481375
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-17-7842C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481375 | ||||||
chr10:80481527
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17-7690A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481527 | ||||||
chr10:80481538
|
T | C | 2 | a0001c0002t0005g0059a0001c0002t0005g0096 | 2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-7679T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481538 | ||||||
chr10:80481612
|
C | T | 5 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0115others(2): Show | 5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-7605C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481612 | ||||||
chr10:80481687
|
G | A | 1 | a0001c0001t0012g0018 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-7530G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481687 | ||||||
chr10:80481689
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17-7528G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481689 | ||||||
chr10:80481728
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-7489C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481728 | ||||||
chr10:80481766
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-7451C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481766 | ||||||
chr10:80481782
|
C | T | 3 | a0001c0001t0018g0121a0001c0001t0033g0124a0001c0001t0057g0120 | 3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-7435C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481782 | ||||||
chr10:80481783
|
G | A | 7 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(4): Show | 7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-7434G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481783 | ||||||
chr10:80481921
|
T | C | 7 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-7296T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481921 | ||||||
chr10:80481945
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-7272G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80481945 | ||||||
chr10:80482054
|
A | G | 8 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(5): Show | 8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-7163A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482054 | ||||||
chr10:80482082
|
G | A | 9 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-7135G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482082 | ||||||
chr10:80482174
|
T | C | 105 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(102): Show | 108 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17-7043T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482174 | ||||||
chr10:80482235
|
A | G | 1 | a0001c0001t0006g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-6982A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482235 | ||||||
chr10:80482347
|
C | G | 1 | a0001c0001t0014g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-6870C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482347 | ||||||
chr10:80482350
|
AATCTCAG others(442): Show |
A | 7 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(4): Show | 7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-6861_-17-6413d others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482350 | |||||
chr10:80482400
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-6817C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482400 | ||||||
chr10:80482413
|
A | C | 1 | a0001c0001t0004g0109 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-17-6804A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482413 | ||||||
chr10:80482477
|
G | C | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6740G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482477 | ||||||
chr10:80482511
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-6706C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482511 | ||||||
chr10:80482537
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0204a0001c0001t0015g0208 | 3 | HG03017.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-17-6680C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482537 | ||||||
chr10:80482547
|
C | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG02004.hp2 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-6670C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482547 | ||||||
chr10:80482659
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-17-6558C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482659 | ||||||
chr10:80482732
|
C | CT | 5 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0002t0005g0238others(2): Show | 5 | HG00639.hp1 HG01515.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-6465dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | |||||
chr10:80482732
|
CT | C | 65 | a0001c0001t0001g0166a0001c0001t0001g0218a0001c0001t0002g0003others(62): Show | 69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-17-6465delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | |||||
chr10:80482732
|
CTT | C | 37 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(34): Show | 38 | HG00642.hp2 HG01069.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-6466_-17-6465d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80482732 | |||||
chr10:80482766
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-17-6451G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80482766 | ||||||
chr10:80483017
|
GAGCCACT others(6): Show |
G | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-6194_-17-6182d others(15): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483017 | |||||
chr10:80483401
|
A | G | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5816A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483401 | ||||||
chr10:80483741
|
C | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5476C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483741 | ||||||
chr10:80483896
|
G | A | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-5321G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483896 | ||||||
chr10:80483911
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17-5279_-17-5266d others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CA | C | 18 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0032others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-5266delA | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAA | C | 15 | a0001c0001t0003g0041a0001c0001t0003g0154a0001c0001t0006g0036others(12): Show | 16 | HG01071.hp2 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-5267_-17-5266d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAA | C | 19 | a0001c0001t0001g0027a0001c0001t0001g0153a0001c0001t0001g0158others(16): Show | 19 | HG00639.hp1 HG00735.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-5268_-17-5266d others(5): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAA | C | 32 | a0001c0001t0001g0071a0001c0001t0001g0155a0001c0001t0001g0165others(29): Show | 32 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-17-5269_-17-5266d others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAA | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0072others(33): Show | 36 | HG00140.hp1 HG00597.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-5270_-17-5266d others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAA | C | 8 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0009g0186others(5): Show | 8 | HG01192.hp1 HG01515.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5271_-17-5266d others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA | C | 6 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0057others(3): Show | 8 | HG02145.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-5272_-17-5266d others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0002g0183a0001c0001t0013g0089a0001c0001t0017g0056others(2): Show | 5 | HG02615.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5273_-17-5266d others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0075a0001c0001t0009g0232a0001c0001t0013g0090others(4): Show | 7 | HG01433.hp1 HG02809.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-5274_-17-5266d others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(3): Show |
C | 19 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0002g0067others(16): Show | 19 | HG00642.hp1 HG00741.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5275_-17-5266d others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(4): Show |
C | 30 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(27): Show | 33 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-5276_-17-5266d others(13): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(5): Show |
C | 18 | a0001c0001t0002g0062a0001c0001t0002g0074a0001c0001t0002g0212others(15): Show | 18 | HG01074.hp1 HG02004.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-5277_-17-5266d others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0004g0102a0001c0001t0016g0224a0001c0001t0016g0225 | 3 | HG02572.hp2 HG03540.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-5278_-17-5266d others(15): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0011g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-17-5280_-17-5266d others(17): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0012g0017a0001c0001t0023g0014a0001c0001t0050g0228 | 3 | HG01081.hp2 HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-17-5282_-17-5266d others(19): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0012g0018a0001c0001t0012g0019a0001c0001t0012g0020others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-5283_-17-5266d others(20): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483911
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0002t0005g0059a0001c0002t0005g0096 | 2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-5284_-17-5266d others(21): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80483911 | |||||
chr10:80483966
|
A | T | 9 | a0001c0001t0007g0046a0001c0001t0007g0054a0001c0001t0007g0077others(6): Show | 9 | HG01175.hp2 HG02486.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-5251A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80483966 | ||||||
chr10:80484073
|
C | T | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-5144C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484073 | ||||||
chr10:80484129
|
C | A | 24 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(21): Show | 25 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-5088C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484129 | ||||||
chr10:80484176
|
C | A | 5 | a0001c0001t0014g0055a0001c0001t0014g0058a0001c0001t0048g0123others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-5041C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484176 | ||||||
chr10:80484200
|
G | A | 113 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-17-5017G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484200 | ||||||
chr10:80484204
|
C | T | 245 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(242): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-17-5013C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484204 | ||||||
chr10:80484230
|
A | G | 237 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-17-4987A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484230 | ||||||
chr10:80484325
|
A | T | 42 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-17-4892A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484325 | ||||||
chr10:80484451
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-4766C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484451 | ||||||
chr10:80484452
|
G | A | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17-4765G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80484452 | ||||||
chr10:80485045
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-17-4172C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485045 | ||||||
chr10:80485047
|
A | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-4170A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485047 | ||||||
chr10:80485200
|
C | CGT | 90 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-17-4006_-17-4005d others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 80485200 | |||||
chr10:80485306
|
G | A | 10 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(7): Show | 10 | HG00642.hp2 HG01081.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-3911G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485306 | ||||||
chr10:80485363
|
T | C | 1 | a0001c0003t0018g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-17-3854T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485363 | ||||||
chr10:80485437
|
C | T | 1 | a0001c0001t0009g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-3780C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485437 | ||||||
chr10:80485520
|
C | A | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-17-3697C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485520 | ||||||
chr10:80485587
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-17-3630C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485587 | ||||||
chr10:80485668
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-17-3549C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485668 | ||||||
chr10:80485721
|
C | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-3496C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485721 | ||||||
chr10:80485752
|
A | G | 7 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(4): Show | 7 | HG01433.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3465A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485752 | ||||||
chr10:80485754
|
C | G | 99 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(96): Show | 104 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.-17-3463C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485754 | ||||||
chr10:80485874
|
C | T | 1 | a0001c0001t0028g0162 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-17-3343C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485874 | ||||||
chr10:80485911
|
A | C | 9 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(6): Show | 9 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-3306A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485911 | ||||||
chr10:80485989
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0015g0195 | 2 | HG00438.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-17-3228A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80485989 | ||||||
chr10:80486343
|
C | T | 3 | a0001c0001t0019g0111a0001c0001t0019g0118a0001c0001t0019g0216 | 3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-17-2874C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486343 | ||||||
chr10:80486409
|
G | A | 1 | a0001c0001t0047g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-2808G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486409 | ||||||
chr10:80486595
|
A | C | 9 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-2622A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486595 | ||||||
chr10:80486611
|
C | G | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-2606C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486611 | ||||||
chr10:80486772
|
A | G | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-2445A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486772 | ||||||
chr10:80486989
|
T | C | 2 | a0001c0001t0002g0136a0001c0001t0053g0137 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-17-2228T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486989 | ||||||
chr10:80486992
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-17-2225C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486992 | ||||||
chr10:80486993
|
A | G | 233 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(230): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-17-2224A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80486993 | ||||||
chr10:80487029
|
C | T | 1 | a0001c0001t0007g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-17-2188C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487029 | ||||||
chr10:80487133
|
C | G | 2 | a0001c0002t0005g0059a0001c0002t0005g0096 | 2 | HG00642.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-17-2084C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487133 | ||||||
chr10:80487283
|
C | G | 1 | a0001c0001t0004g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-17-1934C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487283 | ||||||
chr10:80487288
|
C | T | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1929C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487288 | ||||||
chr10:80487335
|
G | A | 3 | a0001c0001t0018g0121a0001c0001t0033g0124a0001c0001t0057g0120 | 3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-17-1882G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487335 | ||||||
chr10:80487368
|
G | A | 1 | a0001c0001t0022g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-1849G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487368 | ||||||
chr10:80487383
|
A | G | 140 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-17-1834A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487383 | ||||||
chr10:80487466
|
T | C | 1 | a0001c0001t0007g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-17-1751T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487466 | ||||||
chr10:80487517
|
G | A | 2 | a0001c0001t0012g0018a0001c0001t0012g0019 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-17-1700G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487517 | ||||||
chr10:80487531
|
G | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-1686G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487531 | ||||||
chr10:80487620
|
A | G | 3 | a0001c0002t0005g0238a0001c0002t0005g0239a0001c0002t0005g0240 | 3 | HG00639.hp1 HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-1597A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487620 | ||||||
chr10:80487703
|
A | G | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1514A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487703 | ||||||
chr10:80487745
|
G | C | 1 | a0001c0001t0008g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-17-1472G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80487745 | ||||||
chr10:80488025
|
G | A | 5 | a0001c0001t0018g0121a0001c0001t0020g0150a0001c0001t0020g0152others(2): Show | 5 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-1192G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488025 | ||||||
chr10:80488043
|
C | A | 5 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0056others(2): Show | 7 | HG02145.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-1174C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488043 | ||||||
chr10:80488052
|
G | A | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-1165G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488052 | ||||||
chr10:80488078
|
G | A | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1139G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488078 | ||||||
chr10:80488159
|
G | A | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1058G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488159 | ||||||
chr10:80488172
|
C | T | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-1045C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488172 | ||||||
chr10:80488276
|
C | T | 21 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-941C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488276 | ||||||
chr10:80488414
|
T | C | 4 | a0001c0001t0003g0052a0001c0001t0022g0244a0001c0001t0022g0245others(1): Show | 4 | HG01175.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-803T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488414 | ||||||
chr10:80488715
|
A | G | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-17-502A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488715 | ||||||
chr10:80488723
|
A | G | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-494A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488723 | ||||||
chr10:80488729
|
G | T | 1 | a0001c0001t0003g0007 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-17-488G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80488729 | ||||||
chr10:80489051
|
G | A | 1 | a0001c0001t0009g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-17-166G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489051 | ||||||
chr10:80489070
|
T | A | 1 | a0001c0001t0029g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-17-147T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489070 | ||||||
chr10:80489073
|
C | T | 1 | a0001c0001t0006g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-144C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 1/8 | chr10 | 80489073 | ||||||
chr10:80489352
|
C | T | 42 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.81+38C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489352 | ||||||
chr10:80489404
|
A | G | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+90A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489404 | ||||||
chr10:80489426
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.81+112G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489426 | ||||||
chr10:80489996
|
G | A | 203 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(200): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.81+682G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80489996 | ||||||
chr10:80490018
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0044 | 2 | HG01943.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.81+704G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490018 | ||||||
chr10:80490093
|
A | C | 1 | a0001c0001t0012g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.81+779A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490093 | ||||||
chr10:80490203
|
T | C | 2 | a0001c0001t0006g0048a0001c0001t0044g0047 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.81+889T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490203 | ||||||
chr10:80490279
|
C | T | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+965C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490279 | ||||||
chr10:80490486
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+1172G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490486 | ||||||
chr10:80490499
|
A | C | 131 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.81+1185A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490499 | ||||||
chr10:80490769
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0015g0208 | 2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.81+1455T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490769 | ||||||
chr10:80490816
|
A | G | 50 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1502A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80490816 | ||||||
chr10:80491075
|
T | C | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+1761T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491075 | ||||||
chr10:80491085
|
G | T | 1 | a0001c0001t0008g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.81+1771G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491085 | ||||||
chr10:80491128
|
A | G | 1 | a0001c0001t0019g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+1814A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491128 | ||||||
chr10:80491182
|
C | T | 3 | a0001c0002t0021g0184a0001c0002t0021g0185a0001c0002t0021g0187 | 3 | HG01884.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81+1868C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491182 | ||||||
chr10:80491293
|
A | T | 50 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1979A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491293 | ||||||
chr10:80491374
|
C | T | 2 | a0001c0001t0003g0053a0001c0001t0042g0050 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.81+2060C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491374 | ||||||
chr10:80491623
|
T | C | 2 | a0001c0001t0018g0121a0001c0001t0057g0120 | 2 | HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.81+2309T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491623 | ||||||
chr10:80491758
|
T | C | 39 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(36): Show | 41 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.81+2444T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491758 | ||||||
chr10:80491788
|
C | A | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+2474C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80491788 | ||||||
chr10:80492013
|
G | A | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+2699G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492013 | ||||||
chr10:80492200
|
T | A | 2 | a0001c0001t0007g0083a0001c0001t0050g0228 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.81+2886T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492200 | ||||||
chr10:80492440
|
G | C | 1 | a0001c0001t0002g0141 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.81+3126G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492440 | ||||||
chr10:80492582
|
C | G | 21 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3268C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492582 | ||||||
chr10:80492845
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+3531G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492845 | ||||||
chr10:80492941
|
C | T | 4 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0056others(1): Show | 6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+3627C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492941 | ||||||
chr10:80492980
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.81+3666A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80492980 | ||||||
chr10:80493030
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+3716A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493030 | ||||||
chr10:80493199
|
A | G | 1 | a0001c0001t0012g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+3885A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493199 | ||||||
chr10:80493275
|
G | C | 3 | a0001c0001t0002g0062a0001c0001t0002g0074a0001c0001t0009g0073 | 3 | HG02698.hp1 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.81+3961G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493275 | ||||||
chr10:80493378
|
G | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+4064G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493378 | ||||||
chr10:80493758
|
G | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+4444G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493758 | ||||||
chr10:80493879
|
C | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+4565C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493879 | ||||||
chr10:80493945
|
C | A | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.81+4631C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80493945 | ||||||
chr10:80494086
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+4772T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494086 | ||||||
chr10:80494131
|
T | A | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+4817T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494131 | ||||||
chr10:80494154
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.81+4840A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494154 | ||||||
chr10:80494228
|
C | T | 230 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.81+4914C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494228 | ||||||
chr10:80494291
|
A | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(228): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.81+4977A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494291 | ||||||
chr10:80494402
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.81+5088C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494402 | ||||||
chr10:80494632
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+5318G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494632 | ||||||
chr10:80494684
|
G | T | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81+5370G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494684 | ||||||
chr10:80494734
|
C | T | 113 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.81+5420C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494734 | ||||||
chr10:80494804
|
A | G | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+5490A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494804 | ||||||
chr10:80494841
|
AT | A | 4 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0056others(1): Show | 6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+5530delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80494841 | |||||
chr10:80494843
|
T | A | 4 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0056others(1): Show | 6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+5529T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80494843 | ||||||
chr10:80495183
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.81+5869A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495183 | ||||||
chr10:80495293
|
A | G | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+5979A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495293 | ||||||
chr10:80495295
|
C | T | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+5981C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495295 | ||||||
chr10:80495335
|
C | CTG | 4 | a0001c0001t0003g0040a0001c0001t0004g0107a0001c0001t0034g0022others(1): Show | 4 | HG01361.hp1 HG02735.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+6063_81+6064dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495335 | |||||
chr10:80495355
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0010g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81+6045_81+6068del others(24): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495355 | |||||
chr10:80495361
|
GTGTGTGT others(11): Show |
G | 4 | a0001c0001t0006g0048a0001c0001t0014g0058a0001c0001t0044g0047others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+6051_81+6068del others(18): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495361 | |||||
chr10:80495363
|
GTGTGTGT others(9): Show |
G | 104 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(101): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.81+6053_81+6068del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495363 | |||||
chr10:80495365
|
GTGTGTGT others(7): Show |
G | 6 | a0001c0001t0001g0222a0001c0001t0002g0141a0001c0001t0020g0119others(3): Show | 6 | HG00558.hp1 HG01978.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+6055_81+6068del others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495365 | |||||
chr10:80495367
|
GTGTGTGT others(5): Show |
G | 4 | a0001c0001t0001g0191a0001c0001t0009g0186a0001c0001t0022g0244others(1): Show | 4 | HG02622.hp2 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+6057_81+6068del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495367 | |||||
chr10:80495369
|
GTGTGTGT others(3): Show |
G | 14 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(11): Show | 14 | HG00642.hp2 HG01074.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+6059_81+6068del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495369 | |||||
chr10:80495371
|
GTGTGTGT others(1): Show |
G | 7 | a0001c0001t0002g0234a0001c0001t0016g0001a0001c0001t0017g0002others(4): Show | 9 | HG02145.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+6061_81+6068del others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495371 | |||||
chr10:80495373
|
GTGTGTA | G | 50 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+6063_81+6068del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495373 | |||||
chr10:80495375
|
GTGTA | G | 8 | a0001c0001t0004g0109a0001c0001t0007g0046a0001c0001t0007g0082others(5): Show | 8 | HG00639.hp1 HG00642.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+6066_81+6069del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495375 | |||||
chr10:80495377
|
GTA | G | 25 | a0001c0001t0003g0032a0001c0001t0003g0043a0001c0001t0003g0044others(22): Show | 25 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.81+6065_81+6066del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80495377 | |||||
chr10:80495379
|
A | G | 22 | a0001c0001t0002g0092a0001c0001t0002g0095a0001c0001t0003g0007others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.81+6065A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495379 | ||||||
chr10:80495595
|
G | T | 1 | a0001c0002t0005g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81+6281G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495595 | ||||||
chr10:80495641
|
A | G | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+6327A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495641 | ||||||
chr10:80495684
|
A | G | 12 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(9): Show | 12 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+6370A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80495684 | ||||||
chr10:80496018
|
G | A | 120 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(117): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.81+6704G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496018 | ||||||
chr10:80496082
|
T | C | 1 | a0001c0001t0028g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.81+6768T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496082 | ||||||
chr10:80496097
|
A | G | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81+6783A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496097 | ||||||
chr10:80496129
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0009g0073 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81+6815A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496129 | ||||||
chr10:80496161
|
A | G | 15 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+6847A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496161 | ||||||
chr10:80496394
|
C | G | 1 | a0001c0001t0007g0080 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+7080C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496394 | ||||||
chr10:80496406
|
A | G | 1 | a0001c0001t0018g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+7092A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496406 | ||||||
chr10:80496427
|
C | T | 21 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+7113C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496427 | ||||||
chr10:80496464
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+7150G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496464 | ||||||
chr10:80496502
|
T | C | 122 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(119): Show | 123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.81+7188T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496502 | ||||||
chr10:80496718
|
CT | C | 10 | a0001c0001t0001g0009a0001c0001t0002g0136a0001c0001t0002g0138others(7): Show | 10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+7408delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80496718 | |||||
chr10:80496758
|
A | T | 16 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(13): Show | 16 | HG01243.hp1 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+7444A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496758 | ||||||
chr10:80496766
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.81+7452C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496766 | ||||||
chr10:80496782
|
G | C | 8 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(5): Show | 8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+7468G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496782 | ||||||
chr10:80496786
|
T | TATTCTAA others(7): Show |
8 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(5): Show | 8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+7472_81+7473ins others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496786 | ||||||
chr10:80496842
|
A | G | 1 | a0001c0001t0009g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81+7528A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80496842 | ||||||
chr10:80497047
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0177 | 2 | NA18950.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.82-7681C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497047 | ||||||
chr10:80497047
|
C | T | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.82-7681C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497047 | ||||||
chr10:80497364
|
C | G | 130 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(127): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.82-7364C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497364 | ||||||
chr10:80497419
|
G | A | 21 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-7309G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497419 | ||||||
chr10:80497436
|
A | G | 1 | a0001c0002t0005g0241 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82-7292A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497436 | ||||||
chr10:80497814
|
T | C | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.82-6914T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497814 | ||||||
chr10:80497845
|
CTGGGAGG others(5): Show |
C | 1 | a0001c0001t0003g0032 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-6880_82-6869del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80497845 | |||||
chr10:80497954
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.82-6774C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497954 | ||||||
chr10:80497964
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-6764C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497964 | ||||||
chr10:80497980
|
G | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-6748G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80497980 | ||||||
chr10:80498159
|
A | T | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-6569A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498159 | ||||||
chr10:80498265
|
C | G | 9 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(6): Show | 10 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-6463C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498265 | ||||||
chr10:80498390
|
T | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82-6338T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498390 | ||||||
chr10:80498478
|
A | T | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.82-6250A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498478 | ||||||
chr10:80498484
|
C | T | 1 | a0001c0001t0011g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82-6244C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498484 | ||||||
chr10:80498518
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.82-6210G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498518 | ||||||
chr10:80498795
|
C | G | 1 | a0001c0001t0007g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.82-5933C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498795 | ||||||
chr10:80498862
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82-5866A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498862 | ||||||
chr10:80498959
|
G | A | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-5769G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80498959 | ||||||
chr10:80499049
|
G | A | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-5679G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499049 | ||||||
chr10:80499060
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-5668C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499060 | ||||||
chr10:80499461
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.82-5267G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499461 | ||||||
chr10:80499472
|
G | A | 1 | a0001c0001t0030g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.82-5256G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499472 | ||||||
chr10:80499741
|
G | T | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82-4987G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499741 | ||||||
chr10:80499763
|
C | T | 1 | a0001c0002t0005g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82-4965C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499763 | ||||||
chr10:80499764
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82-4964G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80499764 | ||||||
chr10:80499916
|
AAAG | A | 119 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.82-4808_82-4806del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80499916 | |||||
chr10:80499973
|
GGCAGCCA others(9): Show |
G | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-4742_82-4727del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80499973 | |||||
chr10:80500088
|
C | T | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0048others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-4640C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500088 | ||||||
chr10:80500314
|
C | CT | 7 | a0001c0001t0003g0007a0001c0001t0003g0033a0001c0001t0003g0039others(4): Show | 7 | HG00280.hp2 HG01074.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-4382dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTT | C | 16 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(13): Show | 17 | HG00642.hp1 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-4383_82-4382del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTT | C | 31 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(28): Show | 33 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-4384_82-4382del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTTT | C | 16 | a0001c0001t0002g0066a0001c0001t0002g0183a0001c0001t0002g0212others(13): Show | 17 | HG01884.hp1 HG01884.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-4385_82-4382del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTTTT | C | 51 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0072others(48): Show | 52 | HG00621.hp2 HG00642.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.82-4386_82-4382del others(5): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTTTTT | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0153others(96): Show | 100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.82-4387_82-4382del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTTTTTT | C | 6 | a0001c0001t0001g0203a0001c0001t0004g0115a0001c0001t0011g0078others(3): Show | 6 | HG01070.hp2 HG01515.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4388_82-4382del others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500314
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4391_82-4382del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500314 | |||||
chr10:80500351
|
C | T | 2 | a0001c0001t0003g0189a0001c0001t0025g0190 | 2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.82-4377C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500351 | ||||||
chr10:80500543
|
G | A | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.82-4185G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500543 | ||||||
chr10:80500557
|
G | T | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-4171G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500557 | ||||||
chr10:80500571
|
CGCCTCCC others(25): Show |
C | 1 | a0001c0002t0005g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.82-4142_82-4111del others(32): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80500571 | |||||
chr10:80500586
|
T | C | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4142T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500586 | ||||||
chr10:80500702
|
A | T | 2 | a0001c0001t0001g0204a0001c0001t0015g0208 | 2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.82-4026A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80500702 | ||||||
chr10:80501105
|
G | GT | 18 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(15): Show | 18 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-3609dupT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501105 | |||||
chr10:80501105
|
GT | G | 195 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(192): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.82-3609delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501105 | |||||
chr10:80501119
|
T | C | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-3609T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501119 | ||||||
chr10:80501120
|
C | T | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-3608C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501120 | ||||||
chr10:80501121
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-3607T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501121 | ||||||
chr10:80501150
|
G | C | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-3578G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501150 | ||||||
chr10:80501209
|
C | T | 1 | a0001c0001t0040g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82-3519C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501209 | ||||||
chr10:80501214
|
C | T | 1 | a0001c0001t0004g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-3514C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501214 | ||||||
chr10:80501270
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-3458A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501270 | ||||||
chr10:80501285
|
C | A | 1 | a0001c0001t0003g0032 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-3443C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501285 | ||||||
chr10:80501286
|
CT | C | 98 | a0001c0001t0001g0177a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 100 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.82-3422delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501286 | |||||
chr10:80501286
|
CTT | C | 122 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(119): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.82-3423_82-3422del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501286 | |||||
chr10:80501326
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.82-3402A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501326 | ||||||
chr10:80501687
|
A | G | 20 | a0001c0001t0001g0165a0001c0001t0004g0008a0001c0001t0004g0021others(17): Show | 20 | HG00597.hp2 HG02004.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.82-3041A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501687 | ||||||
chr10:80501900
|
CGTT | C | 21 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(18): Show | 21 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-2823_82-2821del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80501900 | |||||
chr10:80501978
|
G | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-2750G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80501978 | ||||||
chr10:80502204
|
G | A | 1 | a0001c0001t0009g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.82-2524G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502204 | ||||||
chr10:80502309
|
C | T | 1 | a0001c0001t0047g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82-2419C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502309 | ||||||
chr10:80502328
|
C | G | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-2400C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502328 | ||||||
chr10:80502552
|
A | C | 3 | a0001c0001t0019g0111a0001c0001t0019g0118a0001c0001t0019g0216 | 3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.82-2176A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502552 | ||||||
chr10:80502651
|
G | T | 25 | a0001c0001t0001g0207a0001c0001t0002g0003a0001c0001t0002g0004others(22): Show | 27 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-2077G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502651 | ||||||
chr10:80502658
|
G | A | 1 | a0001c0001t0033g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-2070G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502658 | ||||||
chr10:80502683
|
C | T | 1 | a0001c0001t0028g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.82-2045C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502683 | ||||||
chr10:80502692
|
G | A | 24 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0141others(21): Show | 25 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.82-2036G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502692 | ||||||
chr10:80502735
|
G | A | 4 | a0001c0001t0016g0001a0001c0001t0017g0002a0001c0001t0017g0056others(1): Show | 6 | HG02145.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1993G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502735 | ||||||
chr10:80502758
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.82-1970G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502758 | ||||||
chr10:80502768
|
A | G | 11 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-1960A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80502768 | ||||||
chr10:80503070
|
C | T | 50 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(47): Show | 53 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.82-1658C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503070 | ||||||
chr10:80503120
|
TG | T | 119 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.82-1604delG | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 80503120 | |||||
chr10:80503214
|
C | T | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82-1514C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503214 | ||||||
chr10:80503757
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.82-971A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503757 | ||||||
chr10:80503826
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82-902G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503826 | ||||||
chr10:80503927
|
G | C | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.82-801G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80503927 | ||||||
chr10:80504082
|
C | G | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.82-646C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504082 | ||||||
chr10:80504126
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-602A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504126 | ||||||
chr10:80504168
|
C | G | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-560C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504168 | ||||||
chr10:80504198
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0072others(18): Show | 21 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.82-530A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504198 | ||||||
chr10:80504390
|
C | T | 1 | a0001c0001t0033g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-338C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504390 | ||||||
chr10:80504524
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-204A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504524 | ||||||
chr10:80504667
|
G | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-61G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 2/8 | chr10 | 80504667 | ||||||
chr10:80504933
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.132+155C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80504933 | ||||||
chr10:80504973
|
G | T | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.132+195G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80504973 | ||||||
chr10:80505013
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.132+235A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505013 | ||||||
chr10:80505057
|
A | G | 139 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(136): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.132+279A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505057 | ||||||
chr10:80505079
|
G | A | 1 | a0001c0001t0047g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.132+301G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505079 | ||||||
chr10:80505096
|
C | T | 10 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(7): Show | 10 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+318C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505096 | ||||||
chr10:80505515
|
A | G | 230 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(227): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.132+737A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80505515 | ||||||
chr10:80506086
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.133-1142C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506086 | ||||||
chr10:80506158
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0063a0001c0001t0002g0064 | 4 | HG01256.hp1 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-1070A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506158 | ||||||
chr10:80506676
|
T | C | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.133-552T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506676 | ||||||
chr10:80506690
|
C | T | 1 | a0001c0001t0009g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133-538C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506690 | ||||||
chr10:80506707
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.133-521C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506707 | ||||||
chr10:80506920
|
C | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-308C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80506920 | ||||||
chr10:80507049
|
C | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.133-179C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80507049 | ||||||
chr10:80507096
|
G | A | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-132G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 3/8 | chr10 | 80507096 | ||||||
chr10:80507480
|
C | G | 22 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+106C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507480 | ||||||
chr10:80507824
|
A | C | 1 | a0001c0001t0002g0138 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.279+450A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507824 | ||||||
chr10:80507855
|
A | G | 41 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(38): Show | 41 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.279+481A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507855 | ||||||
chr10:80507855
|
A | T | 1 | a0001c0001t0007g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.279+481A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507855 | ||||||
chr10:80507881
|
C | G | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+507C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80507881 | ||||||
chr10:80508032
|
A | G | 10 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(7): Show | 10 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+658A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508032 | ||||||
chr10:80508068
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+694C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508068 | ||||||
chr10:80508094
|
G | A | 30 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(27): Show | 32 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.279+720G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508094 | ||||||
chr10:80508119
|
C | CTT | 6 | a0001c0001t0018g0121a0001c0001t0019g0111a0001c0001t0019g0118others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+758_279+759dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 80508119 | |||||
chr10:80508133
|
T | TTG | 8 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(5): Show | 8 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+759_279+760ins others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508133 | ||||||
chr10:80508133
|
T | TTTG | 31 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+759_279+760ins others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508133 | ||||||
chr10:80508140
|
G | A | 1 | a0001c0004t0009g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.279+766G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508140 | ||||||
chr10:80508169
|
G | T | 1 | a0001c0001t0030g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.279+795G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508169 | ||||||
chr10:80508189
|
A | C | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+815A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508189 | ||||||
chr10:80508260
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0175 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.279+886C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508260 | ||||||
chr10:80508364
|
C | T | 3 | a0001c0001t0012g0018a0001c0001t0012g0019a0001c0001t0012g0020 | 3 | HG02723.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.280-937C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508364 | ||||||
chr10:80508365
|
G | A | 2 | a0001c0001t0047g0214a0001c0001t0050g0228 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.280-936G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508365 | ||||||
chr10:80508398
|
G | T | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.280-903G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508398 | ||||||
chr10:80508410
|
G | T | 1 | a0001c0001t0012g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-891G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508410 | ||||||
chr10:80508413
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-888C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508413 | ||||||
chr10:80508684
|
G | T | 1 | a0001c0001t0006g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-617G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508684 | ||||||
chr10:80508687
|
C | T | 3 | a0001c0001t0018g0121a0001c0001t0033g0124a0001c0001t0057g0120 | 3 | HG01243.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.280-614C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508687 | ||||||
chr10:80508834
|
T | A | 1 | a0001c0001t0050g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.280-467T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80508834 | ||||||
chr10:80509021
|
A | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-280A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509021 | ||||||
chr10:80509120
|
G | A | 1 | a0001c0001t0018g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280-181G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509120 | ||||||
chr10:80509175
|
G | A | 19 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(16): Show | 19 | HG00597.hp2 HG02004.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.280-126G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 4/8 | chr10 | 80509175 | ||||||
chr10:80509482
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(121): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.450+11C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509482 | ||||||
chr10:80509705
|
T | C | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.450+234T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509705 | ||||||
chr10:80509816
|
C | T | 1 | a0001c0001t0019g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+345C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509816 | ||||||
chr10:80509837
|
C | G | 1 | a0001c0001t0016g0001 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+366C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509837 | ||||||
chr10:80509855
|
A | G | 222 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(219): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.450+384A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509855 | ||||||
chr10:80509885
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+414C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509885 | ||||||
chr10:80509971
|
A | G | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.450+500A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80509971 | ||||||
chr10:80510023
|
C | T | 4 | a0001c0001t0003g0033a0001c0001t0003g0039a0001c0001t0003g0040others(1): Show | 4 | HG00280.hp2 HG01123.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+552C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510023 | ||||||
chr10:80510092
|
C | G | 228 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(225): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.450+621C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510092 | ||||||
chr10:80510276
|
G | A | 112 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(109): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+805G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510276 | ||||||
chr10:80510412
|
A | G | 1 | a0001c0001t0019g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.450+941A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510412 | ||||||
chr10:80510462
|
C | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.450+991C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510462 | ||||||
chr10:80510519
|
C | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0002g0229others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+1048C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510519 | ||||||
chr10:80510612
|
C | T | 7 | a0001c0001t0014g0058a0001c0001t0018g0121a0001c0001t0019g0111others(4): Show | 7 | HG01243.hp1 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+1141C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510612 | ||||||
chr10:80510648
|
G | A | 22 | a0001c0001t0012g0017a0001c0001t0012g0018a0001c0001t0012g0019others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.450+1177G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510648 | ||||||
chr10:80510715
|
AT | A | 9 | a0001c0001t0007g0046a0001c0001t0007g0054a0001c0001t0007g0077others(6): Show | 9 | HG01175.hp2 HG02486.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+1245delT | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510715 | ||||||
chr10:80510747
|
A | G | 1 | a0001c0001t0011g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.450+1276A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510747 | ||||||
chr10:80510805
|
C | T | 4 | a0001c0001t0012g0018a0001c0001t0012g0019a0001c0001t0012g0020others(1): Show | 4 | HG02723.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1334C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510805 | ||||||
chr10:80510812
|
G | A | 3 | a0001c0001t0017g0002a0001c0001t0017g0056a0001c0001t0017g0057 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1332G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510812 | ||||||
chr10:80510924
|
A | G | 2 | a0001c0001t0002g0092a0001c0001t0002g0095 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.451-1220A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510924 | ||||||
chr10:80510997
|
G | A | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.451-1147G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80510997 | ||||||
chr10:80511085
|
T | A | 2 | a0001c0001t0001g0204a0001c0001t0015g0208 | 2 | HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.451-1059T>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511085 | ||||||
chr10:80511207
|
A | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(8): Show | 12 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-937A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511207 | ||||||
chr10:80511220
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.451-924C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511220 | ||||||
chr10:80511222
|
A | T | 17 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(14): Show | 18 | HG01433.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-922A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511222 | ||||||
chr10:80511418
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0043g0031 | 2 | HG01069.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.451-726C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511418 | ||||||
chr10:80511458
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0015g0195 | 2 | HG00438.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.451-686C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511458 | ||||||
chr10:80511585
|
G | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.451-559G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511585 | ||||||
chr10:80511711
|
C | CCT | 11 | a0001c0001t0001g0011a0001c0001t0001g0169a0001c0001t0001g0203others(8): Show | 12 | HG00558.hp1 HG01074.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-373_451-372dup others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
C | CCTCT | 4 | a0001c0001t0001g0165a0001c0001t0003g0053a0001c0001t0004g0105others(1): Show | 4 | HG01361.hp2 HG02080.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-375_451-372dup others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
C | CCTCTCT | 5 | a0001c0001t0001g0179a0001c0001t0003g0043a0001c0001t0004g0106others(2): Show | 5 | HG00621.hp2 HG02258.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-377_451-372dup others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
C | CCTCTCTC others(3): Show |
4 | a0001c0001t0001g0153a0001c0001t0004g0115a0001c0001t0020g0150others(1): Show | 4 | HG01081.hp1 HG01109.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-381_451-372dup others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
C | CCTCTCTC others(5): Show |
1 | a0001c0001t0001g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-383_451-372dup others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCT | C | 16 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0168others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-373_451-372del others(2): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCT | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0158a0001c0001t0001g0194others(13): Show | 16 | HG00642.hp2 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-375_451-372del others(4): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCT | C | 31 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0177others(28): Show | 32 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.451-377_451-372del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(1): Show |
C | 11 | a0001c0001t0001g0009a0001c0001t0001g0213a0001c0001t0002g0074others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-379_451-372del others(8): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(3): Show |
C | 24 | a0001c0001t0001g0027a0001c0001t0001g0191a0001c0001t0001g0211others(21): Show | 26 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.451-381_451-372del others(10): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(5): Show |
C | 29 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0210others(26): Show | 29 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-383_451-372del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(7): Show |
C | 11 | a0001c0001t0001g0156a0001c0001t0002g0066a0001c0001t0002g0092others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-385_451-372del others(14): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(9): Show |
C | 11 | a0001c0001t0002g0005a0001c0001t0002g0085a0001c0001t0002g0086others(8): Show | 12 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-387_451-372del others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(11): Show |
C | 5 | a0001c0001t0012g0017a0001c0001t0018g0121a0001c0001t0022g0244others(2): Show | 5 | HG01081.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-389_451-372del others(18): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(13): Show |
C | 4 | a0001c0001t0003g0034a0001c0001t0012g0215a0001c0001t0024g0112others(1): Show | 4 | HG01257.hp1 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-391_451-372del others(20): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(17): Show |
C | 6 | a0001c0001t0011g0006a0001c0001t0011g0135a0001c0001t0019g0111others(3): Show | 7 | HG00741.hp1 HG01255.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-395_451-372del others(24): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511711
|
CCTCTCTC others(21): Show |
C | 5 | a0001c0001t0011g0196a0001c0002t0005g0028a0001c0002t0005g0029others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-399_451-372del others(28): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511711 | |||||
chr10:80511726
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.451-418C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511726 | ||||||
chr10:80511761
|
TCTCTCTC others(4): Show |
T | 2 | a0001c0001t0010g0068a0001c0001t0010g0127 | 2 | HG01358.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.451-381_451-371del others(11): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511761 | |||||
chr10:80511763
|
TCTCTCTC others(2): Show |
T | 3 | a0001c0001t0007g0077a0001c0001t0030g0148a0001c0001t0046g0037 | 3 | HG00642.hp1 HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.451-379_451-371del others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511763 | |||||
chr10:80511765
|
TCTCTCTC | T | 4 | a0001c0001t0001g0204a0001c0001t0048g0123a0001c0001t0051g0060others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-377_451-371del others(7): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511765 | |||||
chr10:80511769
|
TCTC | T | 4 | a0001c0001t0001g0220a0001c0001t0003g0041a0001c0001t0006g0114others(1): Show | 4 | HG02922.hp1 HG02922.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-373_451-371del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511769 | |||||
chr10:80511771
|
T | C | 19 | a0001c0001t0002g0003a0001c0001t0002g0063a0001c0001t0002g0064others(16): Show | 21 | HG01109.hp1 HG01167.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.451-373T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511771 | ||||||
chr10:80511771
|
TC | T | 5 | a0001c0001t0001g0071a0001c0001t0008g0199a0001c0001t0039g0130others(2): Show | 5 | HG01099.hp1 HG01258.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-369delC | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511771 | |||||
chr10:80511780
|
T | TTCTTTCT others(9): Show |
1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451-353_451-338dup others(16): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 80511780 | |||||
chr10:80511837
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.451-307G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511837 | ||||||
chr10:80511910
|
C | G | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.451-234C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 5/8 | chr10 | 80511910 | ||||||
chr10:80512302
|
C | T | 1 | a0001c0001t0040g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.576+33C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512302 | ||||||
chr10:80512433
|
T | C | 17 | a0001c0001t0006g0036a0001c0001t0006g0048a0001c0001t0006g0070others(14): Show | 18 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.576+164T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512433 | ||||||
chr10:80512455
|
T | G | 15 | a0001c0002t0005g0024a0001c0002t0005g0025a0001c0002t0005g0028others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.576+186T>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512455 | ||||||
chr10:80512469
|
A | G | 3 | a0001c0001t0014g0055a0001c0001t0048g0123a0001c0003t0014g0122 | 3 | HG02280.hp1 HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.576+200A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512469 | ||||||
chr10:80512590
|
T | C | 3 | a0001c0001t0017g0002a0001c0001t0017g0056a0001c0001t0017g0057 | 4 | HG02145.hp1 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+321T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512590 | ||||||
chr10:80512631
|
C | T | 3 | a0001c0001t0008g0192a0001c0001t0008g0197a0001c0001t0008g0199 | 3 | HG00735.hp1 HG01099.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.576+362C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512631 | ||||||
chr10:80512677
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.576+408A>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512677 | ||||||
chr10:80512750
|
G | A | 3 | a0001c0001t0019g0111a0001c0001t0019g0118a0001c0001t0019g0216 | 3 | HG02970.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.576+481G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80512750 | ||||||
chr10:80512871
|
TTTG | T | 41 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0004g0008others(38): Show | 42 | HG00597.hp2 HG01074.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.576+629_576+631del others(3): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | |||||
chr10:80512871
|
TTTGTTG | T | 15 | a0001c0002t0005g0024a0001c0002t0005g0025a0001c0002t0005g0028others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.576+626_576+631del others(6): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | |||||
chr10:80512871
|
TTTGTTGT others(2): Show |
T | 5 | a0001c0001t0016g0224a0001c0001t0016g0225a0001c0001t0022g0244others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+623_576+631del others(9): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | |||||
chr10:80512871
|
TTTGTTGT others(5): Show |
T | 167 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(164): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.576+620_576+631del others(12): Show |
TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 80512871 | |||||
chr10:80513039
|
C | T | 2 | a0001c0001t0006g0048a0001c0001t0044g0047 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.576+770C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513039 | ||||||
chr10:80513185
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577-834C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513185 | ||||||
chr10:80513323
|
T | C | 188 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(185): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.577-696T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513323 | ||||||
chr10:80513509
|
G | A | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.577-510G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513509 | ||||||
chr10:80513680
|
G | A | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.577-339G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513680 | ||||||
chr10:80513784
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.577-235G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513784 | ||||||
chr10:80513884
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-135G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513884 | ||||||
chr10:80513885
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-134C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80513885 | ||||||
chr10:80514012
|
C | A | 1 | a0001c0001t0016g0001 | 2 | HG02896.hp1 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.577-7C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 6/8 | chr10 | 80514012 | ||||||
chr10:80514486
|
G | T | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.621+423G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514486 | ||||||
chr10:80514666
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.621+603G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514666 | ||||||
chr10:80514818
|
G | A | 4 | a0001c0001t0011g0006a0001c0001t0011g0078a0001c0001t0011g0135others(1): Show | 5 | HG00741.hp1 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+755G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80514818 | ||||||
chr10:80515231
|
C | T | 3 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246 | 3 | HG02622.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.622-973C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515231 | ||||||
chr10:80515335
|
C | T | 1 | a0001c0001t0034g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.622-869C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515335 | ||||||
chr10:80515346
|
C | T | 2 | a0001c0001t0024g0112a0001c0001t0024g0243 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.622-858C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515346 | ||||||
chr10:80515798
|
C | A | 5 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0115others(2): Show | 5 | NA18942.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-406C>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515798 | ||||||
chr10:80515833
|
G | A | 9 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(6): Show | 9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-371G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515833 | ||||||
chr10:80515931
|
A | G | 15 | a0001c0002t0005g0024a0001c0002t0005g0025a0001c0002t0005g0028others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-273A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515931 | ||||||
chr10:80515938
|
G | A | 4 | a0001c0001t0022g0244a0001c0001t0022g0245a0001c0001t0022g0246others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-266G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80515938 | ||||||
chr10:80516009
|
C | T | 15 | a0001c0002t0005g0024a0001c0002t0005g0025a0001c0002t0005g0028others(12): Show | 15 | HG00639.hp1 HG00642.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-195C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516009 | ||||||
chr10:80516025
|
A | G | 9 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(6): Show | 9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-179A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516025 | ||||||
chr10:80516039
|
G | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.622-165G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516039 | ||||||
chr10:80516067
|
G | A | 3 | a0001c0002t0021g0184a0001c0002t0021g0185a0001c0002t0021g0187 | 3 | HG01884.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.622-137G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516067 | ||||||
chr10:80516129
|
C | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG01192.hp1 HG01358.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.622-75C>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 7/8 | chr10 | 80516129 | ||||||
chr10:80516363
|
T | C | 3 | a0001c0001t0012g0018a0001c0001t0012g0019a0001c0001t0012g0020 | 3 | HG02723.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.741+40T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516363 | ||||||
chr10:80516439
|
A | T | 12 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(9): Show | 13 | HG01433.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.741+116A>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516439 | ||||||
chr10:80516525
|
C | T | 1 | a0001c0001t0013g0117 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.741+202C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516525 | ||||||
chr10:80516975
|
C | T | 2 | a0001c0001t0007g0080a0001c0001t0038g0076 | 2 | HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.741+652C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80516975 | ||||||
chr10:80517036
|
C | T | 1 | a0001c0001t0057g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.741+713C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517036 | ||||||
chr10:80517039
|
G | T | 1 | a0001c0001t0027g0094 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.741+716G>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517039 | ||||||
chr10:80517359
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.742-546A>G | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517359 | ||||||
chr10:80517541
|
G | C | 236 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0027others(233): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.742-364G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517541 | ||||||
chr10:80517554
|
C | T | 9 | a0001c0001t0013g0089a0001c0001t0013g0090a0001c0001t0013g0091others(6): Show | 9 | HG01433.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.742-351C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517554 | ||||||
chr10:80517585
|
G | A | 36 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(33): Show | 38 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.742-320G>A | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517585 | ||||||
chr10:80517651
|
G | C | 20 | a0001c0001t0004g0008a0001c0001t0004g0021a0001c0001t0004g0065others(17): Show | 20 | HG00597.hp2 HG02004.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.742-254G>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517651 | ||||||
chr10:80517682
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.742-223T>C | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517682 | ||||||
chr10:80517811
|
C | T | 2 | a0001c0001t0016g0224a0001c0001t0016g0225 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.742-94C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517811 | ||||||
chr10:80517854
|
C | T | 1 | a0001c0001t0008g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.742-51C>T | TSPAN14 | ENSG00000108219.16 | transcript | ENST00000429989.8 | protein_coding | 8/8 | chr10 | 80517854 |