Item | Value |
---|---|
geneid | 6853 |
ensemblid | ENSG00000008056.14 |
hgncid | 11494 |
symbol | SYN1 |
name | synapsin I |
refseq_nuc | NM_006950.3 |
refseq_prot | NP_008881.2 |
ensembl_nuc | ENST00000295987.13 |
ensembl_prot | ENSP00000295987.7 |
mane_status | MANE Select |
chr | chrX |
start | 47571901 |
end | 47619857 |
strand | - |
ver | v1.2 |
region | chrX:47571901-47619857 |
region5000 | chrX:47566901-47624857 |
regionname0 | SYN1_chrX_47571901_47619857 |
regionname5000 | SYN1_chrX_47566901_47624857 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 705 | 264 | 71 | 51 | 104 | 11 | 25 | 77 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0002 | 0/0 | 682 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0003 | 0/0 | 682 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0004 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0005 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0006 | 0/0 | 706 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0007 | 0/0 | 682 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0008 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0009 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0010 | 0/0 | 682 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0011 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0012 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0013 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0014 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0015 | 0/0 | 171 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2118 | 170 | 30 | 31 | 82 | 7 | 18 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0002 | 0/0 | 2118 | 87 | 38 | 18 | 21 | 4 | 6 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0003 | 0/0 | 2118 | 4 | 3 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0004 | 0/0 | 2119 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0005 | 0/0 | 2119 | 2 | 1 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0006 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0007 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0008 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0009 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0010 | 0/0 | 2119 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0011 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0012 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0013 | 0/0 | 2119 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0014 | 0/0 | 2119 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0015 | 0/0 | 2120 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0016 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0017 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0018 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0019 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0020 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
c0021 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1093 | 275 | 73 | 52 | 111 | 11 | 26 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
t0002 | 0/0 | 1093 | 4 | 3 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
t0003 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
t0004 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
t0005 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2118 | 170 | 30 | 31 | 82 | 7 | 18 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0001c0002 | 0/0 | 2118 | 87 | 38 | 18 | 21 | 4 | 6 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0001c0003 | 0/0 | 2118 | 4 | 3 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0001c0018 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0001c0019 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0001c0020 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0002c0004 | 0/0 | 2119 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0002c0013 | 0/0 | 2119 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0003c0005 | 0/0 | 2119 | 2 | 1 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0004c0006 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0005c0021 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0006c0017 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0007c0010 | 0/0 | 2119 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0008c0011 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0009c0016 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0010c0014 | 0/0 | 2119 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0011c0015 | 0/0 | 2120 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0012c0012 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0013c0009 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0014c0008 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 | |
a0015c0007 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3210 | 169 | 29 | 31 | 82 | 7 | 18 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0001t0004 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0002t0001 | 0/0 | 3210 | 83 | 35 | 17 | 21 | 4 | 6 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0002t0002 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0002t0003 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0002t0005 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0003t0001 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0003t0002 | 0/0 | 3210 | 2 | 1 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0018t0001 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0019t0001 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0001c0020t0001 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0002c0004t0001 | 0/0 | 3211 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0002c0013t0001 | 0/0 | 3211 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0003c0005t0001 | 0/0 | 3211 | 2 | 1 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0004c0006t0001 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0005c0021t0001 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0006c0017t0001 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0007c0010t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0008c0011t0001 | 0/0 | 3207 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0009c0016t0001 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0010c0014t0001 | 0/0 | 3211 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0011c0015t0001 | 0/0 | 3212 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0012c0012t0001 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0013c0009t0001 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0014c0008t0001 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
a0015c0007t0001 | 0/0 | 3209 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | copy fasta | chrX | 47566901 | 47624857 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0002t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0018t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0019t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0001c0020t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0002c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0002c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0002c0013t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0003c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0003c0005t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0004c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0004c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0005c0021t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0006c0017t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0007c0010t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0008c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0009c0016t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0010c0014t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0011c0015t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0012c0012t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0013c0009t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0014c0008t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
a0015c0007t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0070 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0220 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01243 | hp1 | a0001 | c0018 | t0001 | g0156 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01496 | hp1 | a0002 | c0004 | t0001 | g0247 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01496 | hp2 | a0010 | c0014 | t0001 | g0057 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0219 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0218 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02148 | hp2 | a0001 | c0002 | t0005 | g0242 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02293 | hp1 | a0014 | c0008 | t0001 | g0211 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0230 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0222 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02735 | hp1 | a0001 | c0020 | t0001 | g0233 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02809 | hp2 | a0007 | c0010 | t0001 | g0196 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03041 | hp2 | a0008 | c0011 | t0001 | g0208 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03516 | hp1 | a0004 | c0006 | t0001 | g0268 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03540 | hp2 | a0004 | c0006 | t0001 | g0269 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0262 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03927 | hp2 | a0011 | c0015 | t0001 | g0168 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | CHB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18942 | hp1 | a0005 | c0021 | t0001 | g0267 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18971 | hp1 | a0012 | c0012 | t0001 | g0099 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18974 | hp1 | a0003 | c0005 | t0001 | g0060 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18990 | hp1 | a0001 | c0019 | t0001 | g0137 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18994 | hp1 | a0002 | c0013 | t0001 | g0159 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19030 | hp1 | a0003 | c0005 | t0001 | g0202 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19030 | hp2 | a0013 | c0009 | t0001 | g0044 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19043 | hp1 | a0009 | c0016 | t0001 | g0188 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19058 | hp1 | a0006 | c0017 | t0001 | g0055 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19084 | hp2 | a0002 | c0004 | t0001 | g0259 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19086 | hp1 | a0015 | c0007 | t0001 | g0180 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | TSI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:47574036 | C | CG | 2 | a0010a0011 | 2 | HG01496.hp2 HG03927.hp2 |
frameshift_variant | HIGH | c.1947dupC | p.Ala650fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 2076/3210 | 1947/2118 | 649/705 | chrX | 47574036 | ||
chrX:47574042 | C | CG | 1 | a0002 | 3 | HG01496.hp1 NA18994.hp1 NA19084.hp2 |
frameshift_variant | HIGH | c.1941dupC | p.Ala648fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 2070/3210 | 1941/2118 | 647/705 | chrX | 47574042 | ||
chrX:47574199 | T | TG | 1 | a0006 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.1784dupC | p.Gly596fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1913/3210 | 1784/2118 | 595/705 | chrX | 47574199 | ||
chrX:47574252 | A | AG | 1 | a0006 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.1731dupC | p.Ser578fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1860/3210 | 1731/2118 | 577/705 | chrX | 47574252 | ||
chrX:47574285 | T | C | 1 | a0004 | 2 | HG03516.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1699A>G | p.Thr567Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1828/3210 | 1699/2118 | 567/705 | chrX | 47574285 | ||
chrX:47574301 | T | TG | 1 | a0011 | 1 | HG03927.hp2 | frameshift_variant | HIGH | c.1682dupC | p.Gln562fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1811/3210 | 1682/2118 | 561/705 | chrX | 47574301 | ||
chrX:47574306 | G | T | 1 | a0012 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.1678C>A | p.Pro560Thr | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1807/3210 | 1678/2118 | 560/705 | chrX | 47574306 | ||
chrX:47574477 | G | C | 1 | a0009 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1507C>G | p.Pro503Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1636/3210 | 1507/2118 | 503/705 | chrX | 47574477 | ||
chrX:47574508 | GTGC | G | 1 | a0008 | 1 | HG03041.hp2 | disruptive_inframe_deletion | MODERATE | c.1473_1475delGCA | p.Gln491del | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1604/3210 | 1473/2118 | 491/705 | chrX | 47574508 | ||
chrX:47574523 | C | CG | 1 | a0007 | 1 | HG02809.hp2 | frameshift_variant | HIGH | c.1460dupC | p.Gln488fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1589/3210 | 1460/2118 | 487/705 | chrX | 47574523 | ||
chrX:47574695 | T | TG | 1 | a0003 | 2 | NA18974.hp1 NA19030.hp1 |
frameshift_variant | HIGH | c.1385dupC | p.Pro463fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 11/13 | 1514/3210 | 1385/2118 | 462/705 | chrX | 47574695 | ||
chrX:47574756 | A | G | 1 | a0013 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1325T>C | p.Leu442Pro | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 11/13 | 1454/3210 | 1325/2118 | 442/705 | chrX | 47574756 | ||
chrX:47575172 | G | GC | 1 | a0006 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.1260dupG | p.Gln421fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 10/13 | 1389/3210 | 1260/2118 | 420/705 | chrX | 47575172 | ||
chrX:47576553 | C | T | 1 | a0014 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.925G>A | p.Asp309Asn | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/13 | 1054/3210 | 925/2118 | 309/705 | chrX | 47576553 | ||
chrX:47607035 | GC | G | 1 | a0015 | 1 | NA19086.hp1 | frameshift_variant&splice_region_variant | HIGH | c.436delG | p.Ala146fs | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/13 | 565/3210 | 436/2118 | 146/705 | chrX | 47607035 | ||
chrX:47619396 | GGCTCCCC others(8): Show |
G | 1 | a0005 | 1 | NA18942.hp1 | disruptive_inframe_deletion | MODERATE | c.318_332delAGGCCGCG others(7): Show |
p.Gly107_Ala111del | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 461/3210 | 318/2118 | 106/705 | chrX | 47619396 | ||
chrX:47619577 | G | C | 1 | a0004 | 2 | HG03516.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.152C>G | p.Ala51Gly | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 281/3210 | 152/2118 | 51/705 | chrX | 47619577 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:47576566 | G | A | 2 | a0001c0003a0001c0018 | 5 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
synonymous_variant | LOW | c.912C>T | p.Ala304Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/13 | 1041/3210 | 912/2118 | 304/705 | chrX | 47576566 | ||
chrX:47605014 | T | C | 1 | a0001c0019 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.738A>G | p.Leu246Leu | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/13 | 867/3210 | 738/2118 | 246/705 | chrX | 47605014 | ||
chrX:47606962 | A | G | 4 | a0001c0002a0001c0003a0001c0020others(1): Show | 94 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
synonymous_variant | LOW | c.510T>C | p.Asn170Asn | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/13 | 639/3210 | 510/2118 | 170/705 | chrX | 47606962 | ||
chrX:47607150 | T | C | 1 | a0001c0020 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.426A>G | p.Lys142Lys | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 2/13 | 555/3210 | 426/2118 | 142/705 | chrX | 47607150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:47572070 | A | G | 1 | a0001c0001t0004 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 794 | chrX | 47572070 | |||||
chrX:47572305 | G | A | 1 | a0001c0002t0005 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*559C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 559 | chrX | 47572305 | |||||
chrX:47572721 | C | T | 2 | a0001c0002t0002a0001c0003t0002 | 4 | HG00735.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 143 | chrX | 47572721 | |||||
chrX:47619833 | A | T | 1 | a0001c0002t0003 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 105 | chrX | 47619833 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:47573032 | A | AG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1983-34dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573032 | ||||||
chrX:47573075 | AC | A | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1983-77delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573075 | ||||||
chrX:47573318 | G | GT | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1983-320dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573318 | ||||||
chrX:47573348 | A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0042others(141): Show | 149 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1983-349T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573348 | ||||||
chrX:47573641 | C | CG | 17 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0081others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982+360dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573641 | ||||||
chrX:47573666 | G | A | 1 | a0004c0006t0001g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1982+336C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573666 | ||||||
chrX:47573922 | A | AG | 1 | a0006c0017t0001g0055 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1982+79dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573922 | ||||||
chrX:47573923 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982+79C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573923 | ||||||
chrX:47575306 | G | T | 1 | a0011c0015t0001g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1159-32C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575306 | ||||||
chrX:47575349 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1159-75A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575349 | ||||||
chrX:47575384 | T | TC | 1 | a0006c0017t0001g0055 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1159-111dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575384 | ||||||
chrX:47575509 | GGTTCTGT others(2): Show |
G | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1159-244_1159-236d others(11): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575509 | ||||||
chrX:47575795 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1158+336T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575795 | ||||||
chrX:47575900 | GCA | G | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1158+229_1158+230d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575900 | ||||||
chrX:47576006 | C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0262 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1158+125G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47576006 | ||||||
chrX:47576013 | T | C | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0002t0001g0037others(5): Show | 8 | HG01081.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158+118A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47576013 | ||||||
chrX:47576104 | A | AC | 1 | a0006c0017t0001g0055 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1158+26dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47576104 | ||||||
chrX:47576240 | AGACAAAG | A | 4 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0002g0220others(1): Show | 4 | HG00735.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1056-14_1056-8delC others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 8/12 | chrX | 47576240 | ||||||
chrX:47576301 | TC | T | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1055+30delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 8/12 | chrX | 47576301 | ||||||
chrX:47576454 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.980+44C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/12 | chrX | 47576454 | ||||||
chrX:47576648 | A | C | 7 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.838-8T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576648 | ||||||
chrX:47576653 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.838-13C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576653 | ||||||
chrX:47576697 | T | TG | 1 | a0010c0014t0001g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.838-58dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576697 | ||||||
chrX:47576931 | G | GA | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.838-292dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576931 | ||||||
chrX:47577078 | C | T | 7 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+361G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577078 | ||||||
chrX:47577179 | A | G | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0002t0001g0037others(5): Show | 8 | HG01081.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+260T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577179 | ||||||
chrX:47577222 | A | G | 2 | a0001c0002t0001g0038a0001c0002t0001g0231 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.837+217T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577222 | ||||||
chrX:47577325 | C | CT | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.837+113dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577325 | ||||||
chrX:47577506 | TG | T | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | splice_region_variant&intron_variant | LOW | c.775-6delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577506 | ||||||
chrX:47577517 | C | CA | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-17dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577517 | ||||||
chrX:47577572 | A | AG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-72dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577572 | ||||||
chrX:47577624 | A | G | 7 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-123T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577624 | ||||||
chrX:47577631 | A | G | 7 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-130T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577631 | ||||||
chrX:47577638 | C | T | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775-137G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577638 | ||||||
chrX:47577641 | G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0231 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.775-140C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577641 | ||||||
chrX:47577777 | T | TC | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-277_775-276ins others(1): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577777 | ||||||
chrX:47577796 | TC | T | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-296delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577796 | ||||||
chrX:47577815 | G | A | 5 | a0001c0001t0001g0085a0001c0001t0001g0140a0001c0001t0001g0142others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-314C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577815 | ||||||
chrX:47577815 | GT | G | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-315delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577815 | ||||||
chrX:47577873 | G | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0048others(72): Show | 77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.775-372C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577873 | ||||||
chrX:47577874 | T | TG | 9 | a0001c0001t0001g0046a0001c0001t0001g0098a0001c0001t0001g0132others(6): Show | 9 | HG01192.hp1 HG01978.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-374dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577874 | ||||||
chrX:47577874 | T | TGG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-375_775-374dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577874 | ||||||
chrX:47577876 | G | C | 5 | a0001c0002t0001g0023a0001c0002t0001g0071a0001c0002t0001g0217others(2): Show | 5 | HG02451.hp1 HG03486.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-375C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577876 | ||||||
chrX:47577958 | A | C | 1 | a0001c0002t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.775-457T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577958 | ||||||
chrX:47578119 | T | TG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-619dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578119 | ||||||
chrX:47578127 | C | T | 7 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-626G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578127 | ||||||
chrX:47578200 | T | TC | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-700dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578200 | ||||||
chrX:47578220 | C | G | 3 | a0001c0003t0001g0012a0001c0003t0001g0024a0001c0018t0001g0156 | 3 | HG01243.hp1 HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.775-719G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578220 | ||||||
chrX:47578372 | C | T | 12 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0170others(9): Show | 12 | HG00741.hp1 HG01069.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.775-871G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578372 | ||||||
chrX:47578431 | G | A | 2 | a0001c0001t0001g0167a0015c0007t0001g0180 | 2 | NA19065.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.775-930C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578431 | ||||||
chrX:47578615 | A | AG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-1115dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578615 | ||||||
chrX:47578646 | T | TG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-1146dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578646 | ||||||
chrX:47578649 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1148C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578649 | ||||||
chrX:47578721 | C | G | 2 | a0001c0002t0001g0071a0001c0002t0001g0262 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.775-1220G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578721 | ||||||
chrX:47578828 | GC | G | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1328delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578828 | ||||||
chrX:47578876 | A | AC | 2 | a0001c0001t0001g0183a0001c0001t0001g0214 | 2 | HG02738.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.775-1376dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578876 | ||||||
chrX:47578893 | TC | T | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-1393delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578893 | ||||||
chrX:47578945 | C | CG | 2 | a0001c0002t0001g0253a0003c0005t0001g0060 | 2 | NA18974.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.775-1445dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578945 | ||||||
chrX:47578991 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-1490C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578991 | ||||||
chrX:47579068 | C | A | 2 | a0001c0003t0001g0012a0001c0018t0001g0156 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.775-1567G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579068 | ||||||
chrX:47579122 | C | CA | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-1622dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579122 | ||||||
chrX:47579125 | A | AC | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-1625dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579125 | ||||||
chrX:47579153 | G | GAC | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-1654_775-1653d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579153 | ||||||
chrX:47579156 | ACAC | A | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775-1658_775-1656d others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579156 | ||||||
chrX:47579358 | A | AG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1858dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579358 | ||||||
chrX:47579408 | T | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0004g0204others(17): Show | 20 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-1907A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579408 | ||||||
chrX:47579410 | TC | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1910delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579410 | ||||||
chrX:47579426 | T | TC | 2 | a0001c0002t0001g0253a0006c0017t0001g0055 | 2 | NA19058.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.775-1926dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579426 | ||||||
chrX:47579465 | T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1965dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579465 | ||||||
chrX:47579475 | T | TG | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-1975dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579475 | ||||||
chrX:47579524 | G | GC | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-2024dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579524 | ||||||
chrX:47579532 | AC | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-2032delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579532 | ||||||
chrX:47579574 | AC | A | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-2074delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579574 | ||||||
chrX:47579587 | TC | T | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-2087delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579587 | ||||||
chrX:47579608 | A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0144 | 2 | NA18961.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.775-2107T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579608 | ||||||
chrX:47579614 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-2113T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579614 | ||||||
chrX:47579615 | TC | T | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-2115delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579615 | ||||||
chrX:47579618 | A | AC | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-2118dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579618 | ||||||
chrX:47579760 | G | GCC | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-2261_775-2260d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579760 | ||||||
chrX:47579849 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.775-2348C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | ||||||
chrX:47579849 | G | GC | 76 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0053others(73): Show | 76 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.775-2349dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | ||||||
chrX:47579849 | G | GCC | 4 | a0001c0001t0001g0148a0001c0002t0001g0249a0001c0002t0001g0253others(1): Show | 4 | HG00438.hp2 HG01433.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-2350_775-2349d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | ||||||
chrX:47579849 | GC | G | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.775-2349delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | ||||||
chrX:47579863 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.775-2362G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579863 | ||||||
chrX:47579879 | G | A | 75 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0053others(72): Show | 75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.775-2378C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579879 | ||||||
chrX:47579924 | CT | C | 1 | a0001c0002t0001g0253 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.775-2424delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579924 | ||||||
chrX:47580013 | T | G | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-2512A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580013 | ||||||
chrX:47580014 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-2513C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580014 | ||||||
chrX:47580185 | C | CT | 5 | a0001c0001t0001g0059a0001c0001t0001g0094a0001c0001t0001g0191others(2): Show | 5 | HG02895.hp1 HG03942.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-2685dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580185 | ||||||
chrX:47580185 | C | CTTT | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-2687_775-2685d others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580185 | ||||||
chrX:47580185 | CT | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0199a0001c0002t0001g0212others(2): Show | 5 | HG01496.hp2 HG02896.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-2685delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580185 | ||||||
chrX:47580201 | T | A | 1 | a0001c0003t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.775-2700A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580201 | ||||||
chrX:47580201 | T | TTA | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.775-2701_775-2700i others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580201 | ||||||
chrX:47580248 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.775-2747G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580248 | ||||||
chrX:47580319 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-2818C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580319 | ||||||
chrX:47580341 | T | C | 1 | a0001c0002t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.775-2840A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580341 | ||||||
chrX:47580354 | G | C | 2 | a0001c0001t0001g0136a0001c0019t0001g0137 | 2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.775-2853C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580354 | ||||||
chrX:47580411 | A | AC | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-2911dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580411 | ||||||
chrX:47580500 | G | A | 1 | a0014c0008t0001g0211 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.775-2999C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580500 | ||||||
chrX:47580605 | TG | T | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.775-3105delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580605 | ||||||
chrX:47580630 | T | TA | 17 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0169others(14): Show | 17 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.775-3130dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580630 | ||||||
chrX:47580630 | T | TAA | 1 | a0001c0003t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.775-3131_775-3130d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580630 | ||||||
chrX:47580630 | TA | T | 4 | a0001c0001t0001g0114a0001c0002t0001g0239a0001c0002t0001g0246others(1): Show | 4 | HG01069.hp1 NA19072.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-3130delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580630 | ||||||
chrX:47580736 | G | C | 2 | a0001c0002t0001g0018a0013c0009t0001g0044 | 2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-3235C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580736 | ||||||
chrX:47580762 | G | C | 82 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(79): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.775-3261C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580762 | ||||||
chrX:47580932 | C | CA | 59 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0051others(56): Show | 59 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.775-3432dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580932 | ||||||
chrX:47580932 | CA | C | 2 | a0001c0002t0001g0212a0010c0014t0001g0057 | 2 | HG01496.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.775-3432delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580932 | ||||||
chrX:47581079 | TC | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-3579delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581079 | ||||||
chrX:47581104 | G | A | 1 | a0003c0005t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775-3603C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581104 | ||||||
chrX:47581163 | T | A | 28 | a0001c0001t0001g0042a0001c0001t0001g0160a0001c0001t0001g0161others(25): Show | 31 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.775-3662A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581163 | ||||||
chrX:47581335 | A | AC | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-3835dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581335 | ||||||
chrX:47581353 | G | C | 26 | a0001c0001t0001g0042a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 29 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.775-3852C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581353 | ||||||
chrX:47581393 | AC | A | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-3893delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581393 | ||||||
chrX:47581495 | A | AT | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-3995dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581495 | ||||||
chrX:47581578 | C | CTGG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4080_775-4078d others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581578 | ||||||
chrX:47581591 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4090C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581591 | ||||||
chrX:47581607 | CG | C | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.775-4107delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581607 | ||||||
chrX:47581670 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.775-4169C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581670 | ||||||
chrX:47581690 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.775-4189C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581690 | ||||||
chrX:47581869 | TG | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4369delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581869 | ||||||
chrX:47581908 | A | AT | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4408dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581908 | ||||||
chrX:47581962 | A | AT | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4462dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581962 | ||||||
chrX:47581977 | GC | G | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4477delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581977 | ||||||
chrX:47582062 | G | A | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 6 | HG02273.hp2 HG02293.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-4561C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582062 | ||||||
chrX:47582081 | T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4581dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582081 | ||||||
chrX:47582098 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4597C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582098 | ||||||
chrX:47582177 | T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4677dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582177 | ||||||
chrX:47582216 | G | GA | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4716_775-4715i others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582216 | ||||||
chrX:47582249 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-4748C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582249 | ||||||
chrX:47582327 | T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4827dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582327 | ||||||
chrX:47582596 | A | AG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-5096dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582596 | ||||||
chrX:47582649 | C | A | 16 | a0001c0001t0001g0043a0001c0001t0001g0169a0001c0001t0001g0170others(13): Show | 16 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-5148G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582649 | ||||||
chrX:47582823 | TC | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-5323delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582823 | ||||||
chrX:47582832 | TC | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-5332delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582832 | ||||||
chrX:47582839 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-5339delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582839 | ||||||
chrX:47582905 | GC | G | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-5405delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582905 | ||||||
chrX:47583028 | AC | A | 1 | a0001c0001t0001g0049 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-5528delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583028 | ||||||
chrX:47583109 | TC | T | 1 | a0001c0001t0001g0157 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.775-5609delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583109 | ||||||
chrX:47583155 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.775-5654G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583155 | ||||||
chrX:47583271 | C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0001g0083others(4): Show | 8 | NA18960.hp1 NA18971.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-5770G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583271 | ||||||
chrX:47583392 | T | TC | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-5892dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583392 | ||||||
chrX:47583513 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.775-6012G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583513 | ||||||
chrX:47583637 | C | CCCTGCAC others(2): Show |
1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-6145_775-6137d others(11): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583637 | ||||||
chrX:47583712 | G | A | 80 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(77): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.775-6211C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583712 | ||||||
chrX:47583841 | G | T | 26 | a0001c0001t0001g0042a0001c0001t0001g0160a0001c0001t0001g0161others(23): Show | 29 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.775-6340C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583841 | ||||||
chrX:47583957 | TG | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-6457delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583957 | ||||||
chrX:47584051 | T | C | 2 | a0001c0002t0001g0018a0013c0009t0001g0044 | 2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-6550A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584051 | ||||||
chrX:47584106 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.775-6605C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584106 | ||||||
chrX:47584130 | G | A | 9 | a0001c0001t0001g0043a0001c0002t0001g0037a0001c0002t0001g0040others(6): Show | 9 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-6629C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584130 | ||||||
chrX:47584207 | G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0217a0001c0002t0001g0265 | 3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-6706C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584207 | ||||||
chrX:47584208 | T | TATTGAGG others(10): Show |
1 | a0001c0003t0002g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.775-6724_775-6708d others(19): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584208 | ||||||
chrX:47584225 | G | GATTGAGG others(27): Show |
8 | a0001c0001t0001g0154a0001c0001t0001g0171a0001c0002t0001g0069others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-6758_775-6725d others(36): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | ||||||
chrX:47584225 | G | GATTGAGG others(61): Show |
6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(3): Show | 6 | HG02273.hp2 HG02293.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-6792_775-6725d others(70): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | ||||||
chrX:47584225 | G | GATTGAGG others(95): Show |
1 | a0001c0002t0001g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.775-6826_775-6725d others(104): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | ||||||
chrX:47584225 | G | GATTGAGG others(163): Show |
3 | a0001c0001t0001g0043a0001c0002t0001g0037a0001c0002t0001g0040 | 3 | HG02145.hp1 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.775-6725_775-6724i others(172): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | ||||||
chrX:47584225 | GATTGAGG others(27): Show |
G | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.775-6758_775-6725d others(36): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | ||||||
chrX:47584244 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-6743A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584244 | ||||||
chrX:47584311 | A | G | 2 | a0001c0001t0004g0204a0001c0003t0002g0220 | 2 | HG00735.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.775-6810T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584311 | ||||||
chrX:47584392 | T | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0169a0001c0001t0001g0170others(16): Show | 19 | HG00099.hp1 HG01243.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-6891A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584392 | ||||||
chrX:47584642 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.775-7141A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584642 | ||||||
chrX:47584845 | G | A | 11 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0165others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.775-7344C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584845 | ||||||
chrX:47584855 | T | TATG | 1 | a0001c0001t0001g0102 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775-7357_775-7355d others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584855 | ||||||
chrX:47584857 | T | C | 1 | a0001c0002t0001g0241 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.775-7356A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584857 | ||||||
chrX:47585025 | G | GC | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-7525dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585025 | ||||||
chrX:47585029 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.775-7528G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585029 | ||||||
chrX:47585229 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.775-7728C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585229 | ||||||
chrX:47585259 | A | AC | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-7759dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585259 | ||||||
chrX:47585264 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.775-7763G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585264 | ||||||
chrX:47585349 | C | CG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-7849dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585349 | ||||||
chrX:47585471 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-7970C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585471 | ||||||
chrX:47585480 | G | C | 132 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(129): Show | 135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-7979C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585480 | ||||||
chrX:47585524 | G | A | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 6 | HG02273.hp2 HG02293.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-8023C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585524 | ||||||
chrX:47585586 | T | C | 132 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(129): Show | 135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-8085A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585586 | ||||||
chrX:47585621 | GC | G | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-8121delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585621 | ||||||
chrX:47585767 | T | G | 3 | a0001c0002t0001g0023a0001c0002t0001g0217a0001c0002t0001g0265 | 3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-8266A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585767 | ||||||
chrX:47585816 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-8316delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585816 | ||||||
chrX:47585824 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.775-8323G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585824 | ||||||
chrX:47585887 | A | G | 132 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(129): Show | 135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-8386T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585887 | ||||||
chrX:47585960 | CG | C | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-8460delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585960 | ||||||
chrX:47586133 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-8633delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586133 | ||||||
chrX:47586243 | CCT | C | 23 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-8744_775-8743d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586243 | ||||||
chrX:47586313 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-8813delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586313 | ||||||
chrX:47586541 | C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 31 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.775-9040G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586541 | ||||||
chrX:47586602 | G | GA | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-9102dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586602 | ||||||
chrX:47586641 | C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | NA18948.hp1 NA18968.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-9140G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586641 | ||||||
chrX:47586695 | C | CT | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-9195dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586695 | ||||||
chrX:47586696 | T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0155 | 2 | HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.775-9195A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586696 | ||||||
chrX:47586744 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-9244delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586744 | ||||||
chrX:47586902 | A | AC | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-9402dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586902 | ||||||
chrX:47586962 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9461T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586962 | ||||||
chrX:47587120 | T | G | 130 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(127): Show | 133 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-9619A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587120 | ||||||
chrX:47587216 | T | TC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9716dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587216 | ||||||
chrX:47587234 | A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9734dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587234 | ||||||
chrX:47587254 | G | A | 84 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(81): Show | 84 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.775-9753C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587254 | ||||||
chrX:47587258 | G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0217a0001c0002t0001g0265 | 3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-9757C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587258 | ||||||
chrX:47587278 | A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9778dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587278 | ||||||
chrX:47587357 | T | TG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9857dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587357 | ||||||
chrX:47587486 | T | TC | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-9986dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587486 | ||||||
chrX:47587510 | T | TC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10010dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587510 | ||||||
chrX:47587530 | G | GA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10030dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587530 | ||||||
chrX:47587583 | A | AT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10083dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587583 | ||||||
chrX:47587737 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.775-10236G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587737 | ||||||
chrX:47587760 | C | G | 82 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(79): Show | 82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.775-10259G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587760 | ||||||
chrX:47587772 | C | A | 4 | a0001c0002t0001g0023a0001c0002t0001g0217a0001c0002t0001g0265others(1): Show | 4 | HG02451.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-10271G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587772 | ||||||
chrX:47587773 | C | A | 4 | a0001c0002t0001g0023a0001c0002t0001g0217a0001c0002t0001g0265others(1): Show | 4 | HG02451.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-10272G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587773 | ||||||
chrX:47587804 | A | AAG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10304_775-1030 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587804 | ||||||
chrX:47587811 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-10311delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587811 | ||||||
chrX:47587830 | C | T | 1 | a0001c0002t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.775-10329G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587830 | ||||||
chrX:47587853 | A | AC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10353dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587853 | ||||||
chrX:47587868 | A | AC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10368dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587868 | ||||||
chrX:47587879 | CT | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10379delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587879 | ||||||
chrX:47587902 | TC | T | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10402delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587902 | ||||||
chrX:47587920 | G | GA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10420dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587920 | ||||||
chrX:47587950 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10450dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587950 | ||||||
chrX:47588010 | GC | G | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-10510delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588010 | ||||||
chrX:47588101 | G | GC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10601dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588101 | ||||||
chrX:47588169 | CA | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10669delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588169 | ||||||
chrX:47588199 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.775-10698C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588199 | ||||||
chrX:47588207 | AC | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10707delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588207 | ||||||
chrX:47588250 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10750dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588250 | ||||||
chrX:47588284 | A | AT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10784dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588284 | ||||||
chrX:47588351 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10851dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588351 | ||||||
chrX:47588359 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10858T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588359 | ||||||
chrX:47588428 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.775-10927G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588428 | ||||||
chrX:47588437 | AG | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10937delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588437 | ||||||
chrX:47588476 | C | T | 22 | a0001c0001t0001g0042a0001c0001t0001g0153a0001c0001t0001g0169others(19): Show | 22 | HG00099.hp1 HG01243.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.775-10975G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588476 | ||||||
chrX:47588486 | G | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0006c0017t0001g0055 | 3 | NA18988.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.775-10985C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588486 | ||||||
chrX:47588525 | C | T | 106 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0050others(103): Show | 109 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.775-11024G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588525 | ||||||
chrX:47588578 | AG | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11078delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588578 | ||||||
chrX:47588605 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.775-11104G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588605 | ||||||
chrX:47588632 | A | AT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11132dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588632 | ||||||
chrX:47588672 | T | TC | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-11172dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588672 | ||||||
chrX:47588697 | T | C | 130 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0048others(127): Show | 133 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-11196A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588697 | ||||||
chrX:47588714 | T | C | 23 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-11213A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588714 | ||||||
chrX:47588743 | T | TG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11243dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588743 | ||||||
chrX:47588749 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-11249delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588749 | ||||||
chrX:47588761 | TG | T | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11261delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588761 | ||||||
chrX:47588798 | GGGGTCAC others(8): Show |
G | 2 | a0001c0001t0001g0084a0001c0001t0001g0100 | 2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.775-11312_775-1129 others(19): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588798 | ||||||
chrX:47588876 | G | A | 49 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052others(46): Show | 49 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.775-11375C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588876 | ||||||
chrX:47588877 | C | A | 49 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052others(46): Show | 49 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.775-11376G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588877 | ||||||
chrX:47588908 | A | G | 135 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0043others(132): Show | 139 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.775-11407T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588908 | ||||||
chrX:47588912 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11412dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588912 | ||||||
chrX:47588939 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-11438C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588939 | ||||||
chrX:47589011 | C | T | 77 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(74): Show | 77 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.775-11510G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589011 | ||||||
chrX:47589017 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.775-11516T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589017 | ||||||
chrX:47589072 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-11572delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589072 | ||||||
chrX:47589117 | T | TG | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-11617dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589117 | ||||||
chrX:47589164 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.775-11663G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589164 | ||||||
chrX:47589165 | G | A | 1 | a0004c0006t0001g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.775-11664C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589165 | ||||||
chrX:47589193 | A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11693dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589193 | ||||||
chrX:47589207 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-11706C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589207 | ||||||
chrX:47589225 | AG | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11725delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589225 | ||||||
chrX:47589258 | C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 149 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.775-11757G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589258 | ||||||
chrX:47589294 | C | CA | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 139 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.775-11794dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | ||||||
chrX:47589294 | C | CAA | 7 | a0001c0001t0001g0105a0001c0001t0001g0129a0001c0001t0001g0166others(4): Show | 7 | HG00408.hp1 HG00558.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-11795_775-1179 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | ||||||
chrX:47589294 | CA | C | 51 | a0001c0001t0001g0042a0001c0001t0001g0081a0001c0001t0001g0095others(48): Show | 54 | HG00099.hp1 HG00735.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.775-11794delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | ||||||
chrX:47589303 | A | AAG | 1 | a0001c0002t0001g0030 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.775-11803_775-1180 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589303 | ||||||
chrX:47589311 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11810T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589311 | ||||||
chrX:47589320 | A | G | 2 | a0001c0001t0001g0088a0001c0003t0002g0222 | 2 | HG02717.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.775-11819T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589320 | ||||||
chrX:47589321 | T | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0119others(2): Show | 5 | NA18979.hp2 NA18988.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-11820A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589321 | ||||||
chrX:47589329 | T | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0150others(5): Show | 8 | HG00438.hp1 HG01358.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-11828A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589329 | ||||||
chrX:47589348 | AT | A | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-11848delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589348 | ||||||
chrX:47589364 | T | C | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.775-11863A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589364 | ||||||
chrX:47589365 | G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.775-11864C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589365 | ||||||
chrX:47589369 | A | G | 2 | a0001c0002t0002g0009a0001c0002t0002g0010 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.775-11868T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589369 | ||||||
chrX:47589389 | C | G | 2 | a0001c0003t0001g0012a0001c0018t0001g0156 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.775-11888G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589389 | ||||||
chrX:47589409 | A | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0170a0001c0001t0001g0172others(1): Show | 4 | HG02622.hp2 NA18984.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-11908T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589409 | ||||||
chrX:47589410 | G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.775-11909C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589410 | ||||||
chrX:47589413 | G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.775-11912C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589413 | ||||||
chrX:47589420 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11919A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589420 | ||||||
chrX:47589427 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11926T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589427 | ||||||
chrX:47589438 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11937G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589438 | ||||||
chrX:47589438 | C | CA | 13 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0163others(10): Show | 13 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-11938dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589438 | ||||||
chrX:47589438 | CA | C | 3 | a0001c0001t0001g0216a0001c0002t0001g0019a0013c0009t0001g0044 | 3 | HG01169.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-11938delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589438 | ||||||
chrX:47589458 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11958_775-1195 others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589458 | ||||||
chrX:47589545 | G | A | 29 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0160others(26): Show | 32 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.775-12044C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589545 | ||||||
chrX:47589561 | A | AC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12061dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589561 | ||||||
chrX:47589584 | A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12084dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589584 | ||||||
chrX:47589595 | C | CA | 25 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0051others(22): Show | 25 | HG00621.hp1 HG01346.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.775-12095dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589595 | ||||||
chrX:47589595 | CA | C | 6 | a0001c0001t0001g0101a0001c0001t0001g0111a0001c0001t0001g0122others(3): Show | 6 | HG01993.hp2 HG03195.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-12095delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589595 | ||||||
chrX:47589623 | A | AC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12123dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589623 | ||||||
chrX:47589656 | GC | G | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12156delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589656 | ||||||
chrX:47589707 | T | TG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12207dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589707 | ||||||
chrX:47589716 | G | GT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12216dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589716 | ||||||
chrX:47589760 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12259A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589760 | ||||||
chrX:47589845 | AC | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12345delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589845 | ||||||
chrX:47589867 | A | ATAACT | 122 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(119): Show | 125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.775-12371_775-1236 others(9): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589867 | ||||||
chrX:47589905 | C | CA | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12405dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589905 | ||||||
chrX:47589964 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12463T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589964 | ||||||
chrX:47589974 | AT | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12474delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589974 | ||||||
chrX:47589985 | AT | A | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-12485delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589985 | ||||||
chrX:47590012 | CA | C | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-12512delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590012 | ||||||
chrX:47590040 | C | G | 1 | a0001c0002t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.775-12539G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590040 | ||||||
chrX:47590045 | A | AG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12545dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590045 | ||||||
chrX:47590059 | T | TC | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12559dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590059 | ||||||
chrX:47590064 | G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0155 | 2 | HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.775-12563C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590064 | ||||||
chrX:47590173 | C | G | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-12672G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590173 | ||||||
chrX:47590212 | GA | G | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-12712delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590212 | ||||||
chrX:47590241 | T | TC | 1 | a0001c0001t0001g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.775-12741dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590241 | ||||||
chrX:47590308 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.775-12807G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590308 | ||||||
chrX:47590332 | AC | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12832delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590332 | ||||||
chrX:47590361 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12860A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590361 | ||||||
chrX:47590409 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-12909delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590409 | ||||||
chrX:47590597 | AG | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-13097delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590597 | ||||||
chrX:47590606 | A | G | 9 | a0001c0001t0001g0045a0001c0001t0004g0204a0001c0002t0001g0069others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-13105T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590606 | ||||||
chrX:47590624 | T | TGG | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-13125_775-1312 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590624 | ||||||
chrX:47590624 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-13124delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590624 | ||||||
chrX:47590745 | G | A | 1 | a0004c0006t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.775-13244C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590745 | ||||||
chrX:47590759 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-13258C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590759 | ||||||
chrX:47590828 | C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(17): Show | 21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.775-13327G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590828 | ||||||
chrX:47590837 | C | A | 9 | a0001c0001t0001g0045a0001c0001t0004g0204a0001c0002t0001g0069others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-13336G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590837 | ||||||
chrX:47590844 | TC | T | 1 | a0001c0001t0001g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.775-13344delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590844 | ||||||
chrX:47590877 | T | C | 88 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(85): Show | 88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.775-13376A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590877 | ||||||
chrX:47590900 | AT | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-13400delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590900 | ||||||
chrX:47591077 | G | GT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-13577dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591077 | ||||||
chrX:47591165 | G | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(17): Show | 21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.775-13664C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591165 | ||||||
chrX:47591181 | T | C | 113 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(110): Show | 116 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.775-13680A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591181 | ||||||
chrX:47591438 | A | AG | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+13539dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591438 | ||||||
chrX:47591442 | C | T | 9 | a0001c0001t0001g0045a0001c0001t0004g0204a0001c0002t0001g0069others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+13536G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591442 | ||||||
chrX:47591550 | G | A | 84 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(81): Show | 84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+13428C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591550 | ||||||
chrX:47591720 | C | CA | 31 | a0001c0001t0001g0116a0001c0001t0001g0160a0001c0001t0001g0162others(28): Show | 34 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.774+13257dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591720 | ||||||
chrX:47591720 | CA | C | 83 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(80): Show | 83 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.774+13257delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591720 | ||||||
chrX:47591744 | T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0119a0006c0017t0001g0055 | 3 | NA18988.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.774+13234A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591744 | ||||||
chrX:47591773 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+13204delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591773 | ||||||
chrX:47591884 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.774+13094T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591884 | ||||||
chrX:47592077 | T | C | 87 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(84): Show | 87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.774+12901A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592077 | ||||||
chrX:47592160 | G | A | 84 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(81): Show | 84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+12818C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592160 | ||||||
chrX:47592166 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.774+12812G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592166 | ||||||
chrX:47592198 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+12780A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592198 | ||||||
chrX:47592259 | AC | A | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+12718delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592259 | ||||||
chrX:47592337 | C | CAAAT | 17 | a0001c0001t0001g0007a0001c0001t0001g0190a0001c0001t0001g0199others(14): Show | 18 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.774+12637_774+1264 others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592337 | ||||||
chrX:47592337 | CAAAT | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.774+12637_774+1264 others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592337 | ||||||
chrX:47592337 | CAAATAAA others(1): Show |
C | 2 | a0001c0002t0001g0019a0013c0009t0001g0044 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.774+12633_774+1264 others(12): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592337 | ||||||
chrX:47592413 | TC | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+12564delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592413 | ||||||
chrX:47592487 | T | C | 1 | a0001c0002t0001g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.774+12491A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592487 | ||||||
chrX:47592554 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+12423delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592554 | ||||||
chrX:47592590 | G | A | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+12388C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592590 | ||||||
chrX:47592696 | T | TA | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+12281dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592696 | ||||||
chrX:47592821 | T | TA | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+12156dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592821 | ||||||
chrX:47592987 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+11991C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592987 | ||||||
chrX:47593043 | T | C | 22 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(19): Show | 25 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.774+11935A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593043 | ||||||
chrX:47593048 | G | GT | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+11929dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593048 | ||||||
chrX:47593143 | CCT | C | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.774+11833_774+1183 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593143 | ||||||
chrX:47593147 | G | T | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.774+11831C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593147 | ||||||
chrX:47593183 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.774+11795G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593183 | ||||||
chrX:47593213 | G | GT | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+11764dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593213 | ||||||
chrX:47593272 | C | CT | 29 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0150others(26): Show | 32 | HG01358.hp1 HG01891.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.774+11705dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593272 | ||||||
chrX:47593272 | C | CTT | 1 | a0001c0002t0001g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.774+11704_774+1170 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593272 | ||||||
chrX:47593272 | CT | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0122 | 2 | NA18992.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.774+11705delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593272 | ||||||
chrX:47593435 | AT | A | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+11542delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593435 | ||||||
chrX:47593528 | C | G | 9 | a0001c0001t0001g0045a0001c0001t0004g0204a0001c0002t0001g0069others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+11450G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593528 | ||||||
chrX:47593626 | T | C | 4 | a0001c0002t0001g0238a0001c0002t0001g0241a0001c0002t0001g0249others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+11352A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593626 | ||||||
chrX:47593738 | TG | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+11239delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593738 | ||||||
chrX:47593757 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+11221G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593757 | ||||||
chrX:47593784 | G | GT | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.774+11193dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593784 | ||||||
chrX:47593888 | AT | A | 1 | a0001c0001t0001g0056 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.774+11089delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593888 | ||||||
chrX:47594191 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.774+10787C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594191 | ||||||
chrX:47594235 | C | CA | 28 | a0001c0001t0001g0098a0001c0001t0001g0121a0001c0001t0001g0160others(25): Show | 31 | HG01192.hp1 HG01361.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.774+10742dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594235 | ||||||
chrX:47594353 | G | GA | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.774+10624dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594353 | ||||||
chrX:47594415 | T | TC | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+10562dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594415 | ||||||
chrX:47594532 | C | CA | 24 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(21): Show | 27 | HG01891.hp1 HG02056.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.774+10445dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594532 | ||||||
chrX:47594532 | CA | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0002t0001g0041others(1): Show | 4 | NA18948.hp1 NA18968.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+10445delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594532 | ||||||
chrX:47594729 | C | CT | 87 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(84): Show | 87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.774+10248dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594729 | ||||||
chrX:47594729 | C | CTT | 1 | a0001c0002t0001g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.774+10247_774+1024 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594729 | ||||||
chrX:47594729 | CT | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0192 | 2 | HG02897.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.774+10248delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594729 | ||||||
chrX:47594753 | G | GT | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+10224dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594753 | ||||||
chrX:47594877 | G | GC | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+10100dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594877 | ||||||
chrX:47594973 | T | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0217a0013c0009t0001g0044 | 3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+10005A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594973 | ||||||
chrX:47595199 | G | A | 84 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(81): Show | 84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+9779C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595199 | ||||||
chrX:47595220 | G | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0217a0013c0009t0001g0044 | 3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+9758C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595220 | ||||||
chrX:47595305 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.774+9673G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595305 | ||||||
chrX:47595396 | T | G | 1 | a0001c0003t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.774+9582A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595396 | ||||||
chrX:47595643 | A | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0217a0013c0009t0001g0044 | 3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+9335T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595643 | ||||||
chrX:47595841 | T | C | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+9137A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595841 | ||||||
chrX:47595947 | A | G | 130 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(127): Show | 134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.774+9031T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595947 | ||||||
chrX:47596051 | A | ACT | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8926_774+8927i others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596051 | ||||||
chrX:47596054 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8924G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596054 | ||||||
chrX:47596055 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8923T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596055 | ||||||
chrX:47596057 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8921G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596057 | ||||||
chrX:47596060 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8918G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596060 | ||||||
chrX:47596061 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8917G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596061 | ||||||
chrX:47596062 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8916G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596062 | ||||||
chrX:47596064 | GCA | G | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8912_774+8913d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596064 | ||||||
chrX:47596067 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8911T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596067 | ||||||
chrX:47596105 | AG | A | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+8872delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596105 | ||||||
chrX:47596246 | C | A | 2 | a0001c0002t0002g0009a0001c0002t0002g0010 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.774+8732G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596246 | ||||||
chrX:47596392 | G | A | 1 | a0012c0012t0001g0099 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.774+8586C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596392 | ||||||
chrX:47596418 | A | T | 2 | a0001c0002t0002g0009a0001c0002t0002g0010 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.774+8560T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596418 | ||||||
chrX:47596457 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.774+8521T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596457 | ||||||
chrX:47596608 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.774+8370T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596608 | ||||||
chrX:47596703 | TA | T | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+8274delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596703 | ||||||
chrX:47596751 | C | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(135): Show | 142 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.774+8227G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596751 | ||||||
chrX:47596798 | C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 8 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+8180G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596798 | ||||||
chrX:47596841 | G | A | 2 | a0001c0002t0001g0019a0013c0009t0001g0044 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.774+8137C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596841 | ||||||
chrX:47597091 | TG | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+7886delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597091 | ||||||
chrX:47597243 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.774+7735C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597243 | ||||||
chrX:47597296 | T | C | 1 | a0013c0009t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.774+7682A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597296 | ||||||
chrX:47597335 | C | CA | 15 | a0001c0001t0001g0054a0001c0001t0001g0200a0001c0002t0001g0036others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.774+7642dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597335 | ||||||
chrX:47597335 | C | CAA | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+7641_774+7642d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597335 | ||||||
chrX:47597335 | CA | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0117a0001c0001t0001g0142others(4): Show | 7 | HG01346.hp2 HG01515.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+7642delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597335 | ||||||
chrX:47597349 | A | AG | 1 | a0001c0002t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.774+7628_774+7629i others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597349 | ||||||
chrX:47597349 | A | G | 21 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(18): Show | 24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+7629T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597349 | ||||||
chrX:47597502 | G | C | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0190others(20): Show | 26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+7476C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597502 | ||||||
chrX:47597518 | C | G | 1 | a0001c0003t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.774+7460G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597518 | ||||||
chrX:47597554 | G | A | 118 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(115): Show | 121 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.774+7424C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597554 | ||||||
chrX:47597598 | G | GA | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.774+7379dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597598 | ||||||
chrX:47597645 | TC | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+7332delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597645 | ||||||
chrX:47597669 | TA | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+7308delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597669 | ||||||
chrX:47597774 | CT | C | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+7203delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597774 | ||||||
chrX:47597944 | CA | C | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+7033delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597944 | ||||||
chrX:47598027 | TA | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6950delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598027 | ||||||
chrX:47598044 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6934C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598044 | ||||||
chrX:47598098 | G | T | 22 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0193others(19): Show | 25 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.774+6880C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598098 | ||||||
chrX:47598148 | AT | A | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6829delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598148 | ||||||
chrX:47598223 | AT | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 8 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+6754delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598223 | ||||||
chrX:47598354 | TA | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6623delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598354 | ||||||
chrX:47598400 | G | GA | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.774+6577dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598400 | ||||||
chrX:47598400 | G | GAA | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+6576_774+6577d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598400 | ||||||
chrX:47598400 | GA | G | 49 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(46): Show | 52 | HG00438.hp2 HG01169.hp1 HG01891.hp1 others(49): Show |
intron_variant | MODIFIER | c.774+6577delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598400 | ||||||
chrX:47598400 | GAA | G | 1 | a0001c0002t0001g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.774+6576_774+6577d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598400 | ||||||
chrX:47598427 | T | TG | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6550dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598427 | ||||||
chrX:47598495 | C | T | 2 | a0001c0001t0001g0171a0011c0015t0001g0168 | 2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.774+6483G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598495 | ||||||
chrX:47598514 | A | G | 2 | a0001c0001t0001g0110a0001c0002t0001g0032 | 2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.774+6464T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598514 | ||||||
chrX:47598582 | CT | C | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6395delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598582 | ||||||
chrX:47598625 | A | AG | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6352dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598625 | ||||||
chrX:47598647 | G | GA | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6330dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598647 | ||||||
chrX:47598827 | A | AAAAT | 5 | a0001c0001t0001g0133a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG02273.hp2 HG02293.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+6147_774+6150d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598827 | ||||||
chrX:47598841 | A | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0217a0013c0009t0001g0044 | 3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+6137T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598841 | ||||||
chrX:47598851 | TA | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6126delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598851 | ||||||
chrX:47598899 | TG | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6078delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598899 | ||||||
chrX:47598904 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.774+6074G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598904 | ||||||
chrX:47598925 | G | A | 45 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(42): Show | 48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+6053C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598925 | ||||||
chrX:47598952 | T | C | 45 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(42): Show | 48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+6026A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598952 | ||||||
chrX:47598961 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.774+6017G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598961 | ||||||
chrX:47599020 | C | A | 1 | a0001c0002t0001g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774+5958G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599020 | ||||||
chrX:47599035 | A | G | 45 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(42): Show | 48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+5943T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599035 | ||||||
chrX:47599035 | AT | A | 1 | a0001c0002t0001g0240 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.774+5942delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599035 | ||||||
chrX:47599229 | A | G | 1 | a0001c0002t0001g0245 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.774+5749T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599229 | ||||||
chrX:47599315 | T | C | 139 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(136): Show | 143 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.774+5663A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599315 | ||||||
chrX:47599376 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.774+5602A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599376 | ||||||
chrX:47599389 | TG | T | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+5588delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599389 | ||||||
chrX:47599549 | A | AT | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+5428dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599549 | ||||||
chrX:47599726 | A | G | 130 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(127): Show | 134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.774+5252T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599726 | ||||||
chrX:47599748 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774+5230C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599748 | ||||||
chrX:47599916 | CA | C | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+5061delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599916 | ||||||
chrX:47600122 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.774+4856T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600122 | ||||||
chrX:47600195 | A | C | 45 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(42): Show | 48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+4783T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600195 | ||||||
chrX:47600202 | G | GT | 7 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0094others(4): Show | 7 | HG00733.hp2 HG03927.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+4775dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600202 | ||||||
chrX:47600373 | A | AT | 1 | a0001c0001t0001g0116 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+4604dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600373 | ||||||
chrX:47600446 | G | A | 9 | a0001c0001t0001g0045a0001c0001t0004g0204a0001c0002t0001g0069others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+4532C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600446 | ||||||
chrX:47600474 | G | C | 44 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(41): Show | 47 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+4504C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600474 | ||||||
chrX:47600526 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+4452T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600526 | ||||||
chrX:47600713 | T | C | 1 | a0001c0002t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.774+4265A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600713 | ||||||
chrX:47600863 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.774+4115A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600863 | ||||||
chrX:47600995 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.774+3983C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600995 | ||||||
chrX:47601086 | CA | C | 1 | a0001c0001t0001g0145 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.774+3891delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601086 | ||||||
chrX:47601450 | T | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(17): Show | 21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.774+3528A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601450 | ||||||
chrX:47601762 | C | G | 43 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(40): Show | 46 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.774+3216G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601762 | ||||||
chrX:47601893 | A | G | 1 | a0001c0020t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.774+3085T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601893 | ||||||
chrX:47602089 | G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG01934.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.774+2889C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602089 | ||||||
chrX:47602150 | C | CG | 1 | a0001c0002t0001g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.774+2827dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602150 | ||||||
chrX:47602150 | C | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0052others(57): Show | 60 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.774+2828G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602150 | ||||||
chrX:47602388 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+2590C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602388 | ||||||
chrX:47602493 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.774+2485C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602493 | ||||||
chrX:47602534 | CG | C | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.774+2443delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602534 | ||||||
chrX:47602570 | A | AG | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+2407dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602570 | ||||||
chrX:47602640 | C | CA | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.774+2337dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602640 | ||||||
chrX:47602640 | CA | C | 2 | a0001c0001t0001g0121a0001c0002t0001g0257 | 2 | HG01981.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.774+2337delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602640 | ||||||
chrX:47602728 | AT | A | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+2249delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602728 | ||||||
chrX:47602734 | A | AG | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.774+2243dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602734 | ||||||
chrX:47602746 | A | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(17): Show | 21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.774+2232T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602746 | ||||||
chrX:47602854 | G | C | 44 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0080others(41): Show | 47 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+2124C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602854 | ||||||
chrX:47602876 | TG | T | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.774+2101delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602876 | ||||||
chrX:47602979 | A | AT | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.774+1998dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602979 | ||||||
chrX:47603013 | AT | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0081a0001c0001t0004g0204others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.774+1964delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603013 | ||||||
chrX:47603134 | TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+1843delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603134 | ||||||
chrX:47603168 | G | GT | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.774+1809dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603168 | ||||||
chrX:47603177 | A | AC | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+1800_774+1801i others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603177 | ||||||
chrX:47603217 | G | GA | 1 | a0001c0002t0001g0257 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+1760dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603217 | ||||||
chrX:47603231 | C | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0052others(57): Show | 60 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.774+1747G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603231 | ||||||
chrX:47603232 | T | G | 107 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(104): Show | 110 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.774+1746A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603232 | ||||||
chrX:47603236 | G | GC | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.774+1741dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603236 | ||||||
chrX:47603318 | T | TC | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.774+1659dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603318 | ||||||
chrX:47603321 | CA | C | 1 | a0001c0002t0001g0257 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+1656delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603321 | ||||||
chrX:47603329 | T | TG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.774+1648dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603329 | ||||||
chrX:47603371 | A | AT | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.774+1606dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603371 | ||||||
chrX:47603385 | TG | T | 1 | a0001c0001t0001g0145 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.774+1592delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603385 | ||||||
chrX:47603397 | A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0001g0107 | 3 | HG01169.hp2 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.774+1581T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603397 | ||||||
chrX:47603457 | AT | A | 3 | a0001c0001t0001g0145a0003c0005t0001g0060a0005c0021t0001g0267 | 3 | NA18942.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.774+1520delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603457 | ||||||
chrX:47603462 | TA | T | 1 | a0001c0001t0001g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.774+1515delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603462 | ||||||
chrX:47603509 | G | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0045others(76): Show | 83 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.774+1469C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603509 | ||||||
chrX:47603730 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+1248T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603730 | ||||||
chrX:47603779 | T | TG | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.774+1198dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603779 | ||||||
chrX:47603889 | A | ATT | 2 | a0001c0002t0002g0009a0001c0002t0002g0010 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.774+1087_774+1088d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603889 | ||||||
chrX:47603890 | T | TTA | 2 | a0001c0001t0001g0045a0001c0001t0001g0121 | 2 | HG01081.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.774+1086_774+1087d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603890 | ||||||
chrX:47603890 | T | TTTTA | 16 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(13): Show | 17 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.774+1087_774+1088i others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603890 | ||||||
chrX:47603892 | A | T | 2 | a0001c0003t0001g0012a0001c0018t0001g0156 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.774+1086T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603892 | ||||||
chrX:47603904 | ATAT | A | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+1071_774+1073d others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603904 | ||||||
chrX:47603906 | A | AT | 4 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0001g0163others(1): Show | 4 | HG01109.hp1 HG02056.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+1071dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | ||||||
chrX:47603906 | A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0124 | 2 | HG00558.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.774+1072T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | ||||||
chrX:47603906 | AT | A | 16 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0052others(13): Show | 16 | HG00597.hp1 HG00621.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.774+1071delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | ||||||
chrX:47603906 | ATT | A | 1 | a0004c0006t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.774+1070_774+1071d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | ||||||
chrX:47603907 | T | TA | 82 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0050others(79): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.774+1070_774+1071i others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603907 | ||||||
chrX:47603908 | T | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0048others(61): Show | 68 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.774+1070A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603908 | ||||||
chrX:47603909 | T | A | 79 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0049others(76): Show | 79 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.774+1069A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603909 | ||||||
chrX:47603910 | T | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0058others(30): Show | 34 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.774+1068A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603910 | ||||||
chrX:47603911 | T | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0091a0001c0001t0001g0148others(3): Show | 6 | HG00438.hp2 HG00597.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1067A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603911 | ||||||
chrX:47603912 | T | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0199others(22): Show | 26 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.774+1066A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603912 | ||||||
chrX:47603913 | T | A | 2 | a0001c0003t0001g0012a0001c0018t0001g0156 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.774+1065A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603913 | ||||||
chrX:47603914 | T | A | 3 | a0001c0002t0001g0073a0001c0002t0002g0009a0001c0002t0002g0010 | 3 | HG02723.hp1 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.774+1064A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603914 | ||||||
chrX:47603938 | G | A | 21 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0193others(18): Show | 24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+1040C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603938 | ||||||
chrX:47603986 | CA | C | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+991delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603986 | ||||||
chrX:47604151 | C | T | 1 | a0001c0002t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.774+827G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604151 | ||||||
chrX:47604161 | G | A | 21 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0193others(18): Show | 24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+817C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604161 | ||||||
chrX:47604168 | C | T | 2 | a0001c0002t0001g0014a0001c0002t0001g0015 | 2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.774+810G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604168 | ||||||
chrX:47604179 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.774+799C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604179 | ||||||
chrX:47604198 | C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172 | 3 | HG02273.hp2 NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.774+780G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604198 | ||||||
chrX:47604232 | A | AC | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+745dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604232 | ||||||
chrX:47604313 | C | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0109others(16): Show | 20 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+665G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604313 | ||||||
chrX:47604345 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.774+633G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604345 | ||||||
chrX:47604410 | GC | G | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.774+567delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604410 | ||||||
chrX:47604441 | C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0199a0001c0001t0001g0201others(15): Show | 19 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.774+537G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604441 | ||||||
chrX:47604488 | T | C | 1 | a0004c0006t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.774+490A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604488 | ||||||
chrX:47604892 | GC | G | 75 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0001g0080others(72): Show | 75 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.774+85delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604892 | ||||||
chrX:47605398 | G | A | 1 | a0001c0003t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.528-19C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605398 | ||||||
chrX:47605416 | C | CT | 1 | a0001c0002t0001g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.528-38_528-37insA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605416 | ||||||
chrX:47605615 | CA | C | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.528-237delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605615 | ||||||
chrX:47605713 | C | A | 4 | a0001c0001t0001g0042a0001c0002t0001g0013a0001c0002t0002g0009others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-334G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605713 | ||||||
chrX:47605893 | A | T | 20 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0062others(17): Show | 20 | HG00423.hp2 HG00544.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-514T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605893 | ||||||
chrX:47605901 | C | CT | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.528-523dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605901 | ||||||
chrX:47605901 | CT | C | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.528-523delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605901 | ||||||
chrX:47605908 | T | C | 3 | a0001c0002t0001g0013a0001c0002t0002g0009a0001c0002t0002g0010 | 3 | HG01891.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.528-529A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605908 | ||||||
chrX:47605923 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.528-544G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605923 | ||||||
chrX:47605927 | C | G | 3 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0040 | 3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.528-548G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605927 | ||||||
chrX:47605948 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.528-569C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605948 | ||||||
chrX:47605971 | T | C | 3 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0040 | 3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.528-592A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605971 | ||||||
chrX:47605979 | GC | G | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.528-601delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605979 | ||||||
chrX:47606247 | G | A | 1 | a0001c0020t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.527+698C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606247 | ||||||
chrX:47606293 | TTC | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0078 | 2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.527+650_527+651del others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606293 | ||||||
chrX:47606295 | C | CT | 83 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(80): Show | 86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.527+649dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606295 | ||||||
chrX:47606295 | C | CTT | 1 | a0001c0002t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.527+648_527+649dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606295 | ||||||
chrX:47606295 | CT | C | 1 | a0013c0009t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.527+649delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606295 | ||||||
chrX:47606296 | T | C | 3 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0040 | 3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527+649A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606296 | ||||||
chrX:47606445 | TG | T | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.527+499delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606445 | ||||||
chrX:47606549 | A | AC | 4 | a0001c0001t0001g0066a0001c0001t0001g0089a0001c0001t0001g0132others(1): Show | 4 | HG01099.hp1 HG01978.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+395dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606549 | ||||||
chrX:47606730 | A | AAT | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.527+213_527+214dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606730 | ||||||
chrX:47606747 | A | AT | 1 | a0001c0002t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.527+197dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606747 | ||||||
chrX:47606747 | A | T | 2 | a0001c0002t0001g0016a0001c0002t0001g0036 | 2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.527+198T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606747 | ||||||
chrX:47606748 | TA | T | 2 | a0001c0002t0001g0033a0004c0006t0001g0269 | 2 | HG03540.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.527+196delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606748 | ||||||
chrX:47606749 | A | AT | 5 | a0001c0002t0001g0015a0001c0002t0001g0017a0001c0002t0001g0026others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+195dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606749 | ||||||
chrX:47606749 | A | T | 18 | a0001c0002t0001g0014a0001c0002t0001g0016a0001c0002t0001g0018others(15): Show | 18 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.527+196T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606749 | ||||||
chrX:47606751 | A | ATATATAT | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.527+193_527+194ins others(7): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606751 | A | ATATATT | 3 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0040 | 3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527+193_527+194ins others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606751 | A | ATATATTT others(1): Show |
1 | a0013c0009t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.527+193_527+194ins others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606751 | A | ATTTTTTT | 2 | a0001c0002t0002g0009a0001c0002t0002g0010 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.527+187_527+193dup others(7): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606751 | A | T | 84 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0076others(81): Show | 87 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.527+194T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606751 | AT | A | 1 | a0004c0006t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.527+193delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | ||||||
chrX:47606752 | T | TA | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.527+192_527+193ins others(1): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606752 | ||||||
chrX:47606752 | T | TATATATA | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527+192_527+193ins others(7): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606752 | ||||||
chrX:47606753 | T | A | 6 | a0001c0001t0001g0043a0001c0001t0001g0081a0001c0001t0001g0119others(3): Show | 6 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.527+192A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606753 | ||||||
chrX:47606794 | C | T | 1 | a0002c0004t0001g0259 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.527+151G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606794 | ||||||
chrX:47606878 | TC | T | 1 | a0015c0007t0001g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.527+66delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606878 | ||||||
chrX:47607047 | GA | G | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.436-12delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 2/12 | chrX | 47607047 | ||||||
chrX:47607114 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.435+27G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 2/12 | chrX | 47607114 | ||||||
chrX:47607217 | A | T | 1 | a0001c0002t0001g0029 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.378-19T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607217 | ||||||
chrX:47607244 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.378-46C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607244 | ||||||
chrX:47607479 | T | C | 95 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0002t0001g0002others(92): Show | 98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-281A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607479 | ||||||
chrX:47607519 | C | T | 95 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0002t0001g0002others(92): Show | 98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-321G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607519 | ||||||
chrX:47607521 | C | T | 3 | a0001c0001t0001g0045a0004c0006t0001g0268a0004c0006t0001g0269 | 3 | HG01081.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.378-323G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607521 | ||||||
chrX:47607551 | C | T | 10 | a0001c0002t0001g0002a0001c0002t0001g0021a0001c0002t0001g0022others(7): Show | 13 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.378-353G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607551 | ||||||
chrX:47607560 | C | T | 6 | a0001c0002t0001g0013a0001c0002t0001g0037a0001c0002t0001g0038others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-362G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607560 | ||||||
chrX:47607616 | G | A | 24 | a0001c0002t0001g0002a0001c0002t0001g0021a0001c0002t0001g0022others(21): Show | 27 | HG00099.hp1 HG00735.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.378-418C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607616 | ||||||
chrX:47607727 | G | GA | 18 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0079others(15): Show | 18 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.378-530dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | ||||||
chrX:47607727 | G | GAA | 74 | a0001c0002t0001g0002a0001c0002t0001g0013a0001c0002t0001g0014others(71): Show | 77 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.378-531_378-530dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | ||||||
chrX:47607727 | G | GAAA | 9 | a0001c0002t0001g0015a0001c0002t0001g0034a0001c0002t0001g0219others(6): Show | 9 | HG00544.hp1 HG01516.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.378-532_378-530dup others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | ||||||
chrX:47607727 | G | GAAAA | 2 | a0004c0006t0001g0268a0004c0006t0001g0269 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.378-533_378-530dup others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | ||||||
chrX:47607727 | GA | G | 5 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0119others(2): Show | 5 | HG01167.hp1 HG02965.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-530delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | ||||||
chrX:47607746 | C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0003t0002g0220others(1): Show | 4 | HG00735.hp2 NA18942.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-548G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607746 | ||||||
chrX:47607757 | G | A | 1 | a0013c0009t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-559C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607757 | ||||||
chrX:47608001 | G | A | 85 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(82): Show | 88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.378-803C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608001 | ||||||
chrX:47608176 | TG | T | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.378-979delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608176 | ||||||
chrX:47608223 | A | AAAGGAAG others(1): Show |
1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.378-1033_378-1026d others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608223 | ||||||
chrX:47608245 | AGGAAGGA others(39): Show |
A | 1 | a0001c0002t0001g0260 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.378-1093_378-1048d others(48): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608245 | ||||||
chrX:47608259 | GAAGGAAG others(19): Show |
G | 6 | a0001c0002t0001g0035a0001c0002t0001g0041a0001c0002t0001g0238others(3): Show | 6 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-1087_378-1062d others(28): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608259 | ||||||
chrX:47608263 | GAAGGAAG others(15): Show |
G | 38 | a0001c0002t0001g0016a0001c0002t0001g0018a0001c0002t0001g0019others(35): Show | 38 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.378-1087_378-1066d others(24): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608263 | ||||||
chrX:47608267 | GAAGGAAG others(11): Show |
G | 32 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0017others(29): Show | 35 | HG01346.hp1 HG01361.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.378-1087_378-1070d others(20): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608267 | ||||||
chrX:47608271 | GAAGGAAG others(7): Show |
G | 7 | a0001c0001t0001g0042a0001c0002t0001g0015a0001c0002t0001g0021others(4): Show | 7 | HG00099.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1087_378-1074d others(16): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608271 | ||||||
chrX:47608275 | GAAGGAAG others(3): Show |
G | 3 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0002g0220 | 3 | HG00735.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.378-1087_378-1078d others(12): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608275 | ||||||
chrX:47608279 | GAAGGAA | G | 8 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0207others(5): Show | 8 | HG00642.hp1 HG01081.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-1087_378-1082d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608279 | ||||||
chrX:47608283 | G | A | 2 | a0001c0001t0001g0136a0001c0019t0001g0137 | 2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.378-1085C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608283 | ||||||
chrX:47608283 | GAA | G | 13 | a0001c0001t0001g0045a0001c0001t0001g0190a0001c0001t0001g0193others(10): Show | 13 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.378-1087_378-1086d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608283 | ||||||
chrX:47608288 | A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0147others(6): Show | 10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1090T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608288 | ||||||
chrX:47608289 | A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0147others(6): Show | 10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1091T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608289 | ||||||
chrX:47608289 | AGG | A | 107 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0134others(104): Show | 110 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.378-1093_378-1092d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608289 | ||||||
chrX:47608290 | G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0147others(6): Show | 10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1092C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608290 | ||||||
chrX:47608291 | G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0147others(6): Show | 10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1093C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGAAG others(21): Show |
1 | a0001c0001t0001g0157 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.378-1094_378-1093i others(30): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGAAG others(17): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG00597.hp2 NA18964.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(26): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGAAG others(13): Show |
14 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0085others(11): Show | 15 | HG00280.hp1 HG00558.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(22): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGAAG others(9): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0076others(32): Show | 39 | HG00735.hp1 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(18): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGAAG others(5): Show |
36 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0059others(33): Show | 38 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGGGA others(1): Show |
39 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0048others(36): Show | 40 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GAAGGGGG others(2): Show |
1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.378-1094_378-1093i others(11): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608291 | G | GGGAA | 20 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0053others(17): Show | 21 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.378-1097_378-1094d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | ||||||
chrX:47608507 | G | C | 3 | a0001c0002t0001g0013a0001c0002t0002g0009a0001c0002t0002g0010 | 3 | HG01891.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.378-1309C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608507 | ||||||
chrX:47608583 | TG | T | 1 | a0001c0001t0001g0081 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.378-1386delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608583 | ||||||
chrX:47608673 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.378-1475G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608673 | ||||||
chrX:47608695 | CG | C | 1 | a0001c0002t0001g0250 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.378-1498delC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608695 | ||||||
chrX:47608824 | A | AGGGGG | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.378-1631_378-1627d others(7): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608824 | ||||||
chrX:47608863 | A | G | 95 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0002t0001g0002others(92): Show | 98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-1665T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608863 | ||||||
chrX:47608886 | G | GAC | 63 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0138others(60): Show | 67 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.378-1690_378-1689d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608886 | G | GACAC | 49 | a0001c0001t0001g0148a0001c0001t0001g0205a0001c0001t0001g0206others(46): Show | 49 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.378-1692_378-1689d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608886 | G | GACACAC | 2 | a0001c0001t0001g0043a0001c0002t0001g0261 | 2 | HG00408.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.378-1694_378-1689d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608886 | G | GACACACA others(1): Show |
2 | a0001c0002t0001g0040a0001c0002t0001g0265 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.378-1696_378-1689d others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608886 | GAC | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0054others(7): Show | 10 | HG00597.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1690_378-1689d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608886 | GACAC | G | 6 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG01081.hp1 HG02015.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-1692_378-1689d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | ||||||
chrX:47608921 | A | ACAC | 1 | a0001c0001t0001g0189 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.378-1724_378-1723i others(5): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608921 | ||||||
chrX:47608935 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378-1737G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608935 | ||||||
chrX:47608969 | CA | C | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.378-1772delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608969 | ||||||
chrX:47609004 | T | TCACACAC others(1): Show |
1 | a0004c0006t0001g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378-1807_378-1806i others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609004 | ||||||
chrX:47609005 | G | C | 1 | a0004c0006t0001g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378-1807C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GAC | 14 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0149others(11): Show | 14 | HG00558.hp1 HG01358.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.378-1809_378-1808d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACAC | 52 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0042others(49): Show | 53 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.378-1811_378-1808d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACAC | 38 | a0001c0001t0001g0173a0001c0002t0001g0015a0001c0002t0001g0026others(35): Show | 38 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.378-1813_378-1808d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(1): Show |
17 | a0001c0002t0001g0016a0001c0002t0001g0020a0001c0002t0001g0029others(14): Show | 17 | HG00544.hp1 HG00738.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.378-1815_378-1808d others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(3): Show |
11 | a0001c0002t0001g0002a0001c0002t0001g0021a0001c0002t0001g0022others(8): Show | 14 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.378-1817_378-1808d others(12): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(5): Show |
7 | a0001c0002t0001g0018a0001c0002t0001g0070a0001c0002t0001g0071others(4): Show | 7 | HG00099.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1819_378-1808d others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(7): Show |
1 | a0001c0002t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378-1821_378-1808d others(16): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(9): Show |
1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.378-1823_378-1808d others(18): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | G | GACACACA others(11): Show |
1 | a0001c0002t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.378-1825_378-1808d others(20): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | GAC | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG00597.hp1 HG00621.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1809_378-1808d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609005 | GACAC | G | 4 | a0001c0001t0001g0076a0001c0002t0001g0037a0001c0002t0001g0038others(1): Show | 4 | HG01123.hp2 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-1811_378-1808d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | ||||||
chrX:47609131 | G | A | 83 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(80): Show | 86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.378-1933C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609131 | ||||||
chrX:47609155 | CT | C | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.378-1958delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609155 | ||||||
chrX:47609343 | T | C | 60 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(57): Show | 60 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.378-2145A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609343 | ||||||
chrX:47609345 | T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG00558.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.378-2147A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609345 | ||||||
chrX:47609346 | GA | G | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.378-2149delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609346 | ||||||
chrX:47609382 | GGGCTGA | G | 1 | a0013c0009t0001g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-2190_378-2185d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609382 | ||||||
chrX:47609432 | C | T | 82 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(79): Show | 85 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.378-2234G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609432 | ||||||
chrX:47609575 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-2377G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609575 | ||||||
chrX:47609889 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.378-2691C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609889 | ||||||
chrX:47609956 | G | GT | 1 | a0003c0005t0001g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.378-2759dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609956 | ||||||
chrX:47610034 | G | A | 8 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG02074.hp1 HG02273.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-2836C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610034 | ||||||
chrX:47610199 | C | T | 1 | a0001c0002t0001g0020 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.378-3001G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610199 | ||||||
chrX:47610200 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.378-3002C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610200 | ||||||
chrX:47610366 | CCT | C | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.378-3170_378-3169d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610366 | ||||||
chrX:47610420 | T | C | 1 | a0001c0002t0001g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.378-3222A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610420 | ||||||
chrX:47610501 | G | A | 1 | a0004c0006t0001g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378-3303C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610501 | ||||||
chrX:47610739 | T | C | 4 | a0001c0002t0001g0013a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3541A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610739 | ||||||
chrX:47610953 | A | G | 1 | a0001c0002t0003g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.378-3755T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610953 | ||||||
chrX:47610958 | C | T | 4 | a0001c0002t0001g0013a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3760G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610958 | ||||||
chrX:47610959 | G | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | NA18961.hp1 NA18970.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.378-3761C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610959 | ||||||
chrX:47611047 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-3849T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611047 | ||||||
chrX:47611084 | A | G | 4 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0003t0001g0012others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3886T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611084 | ||||||
chrX:47611181 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.378-3983T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611181 | ||||||
chrX:47611326 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-4128T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611326 | ||||||
chrX:47611430 | C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0045others(85): Show | 91 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.378-4232G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611430 | ||||||
chrX:47611577 | G | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(74): Show | 80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.378-4379C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611577 | ||||||
chrX:47611859 | CCAAAGAA others(5): Show |
C | 77 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(74): Show | 80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.378-4673_378-4662d others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611859 | ||||||
chrX:47611890 | AC | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.378-4693delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611890 | ||||||
chrX:47611916 | A | C | 1 | a0001c0003t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.378-4718T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611916 | ||||||
chrX:47611961 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378-4763T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611961 | ||||||
chrX:47612228 | G | C | 1 | a0001c0002t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378-5030C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612228 | ||||||
chrX:47612232 | T | C | 4 | a0001c0001t0001g0042a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-5034A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612232 | ||||||
chrX:47612367 | T | TG | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.378-5170dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612367 | ||||||
chrX:47612538 | T | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0045others(86): Show | 92 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.378-5340A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612538 | ||||||
chrX:47612557 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.378-5359C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612557 | ||||||
chrX:47612678 | G | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0003c0005t0001g0060 | 3 | NA18952.hp1 NA18974.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.378-5480C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612678 | ||||||
chrX:47612804 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.378-5606G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612804 | ||||||
chrX:47612819 | A | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0045others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.378-5621T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612819 | ||||||
chrX:47612899 | G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | NA19060.hp1 NA19070.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.378-5701C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612899 | ||||||
chrX:47612902 | G | A | 1 | a0001c0002t0003g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.378-5704C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612902 | ||||||
chrX:47612990 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.378-5792C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612990 | ||||||
chrX:47613005 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.378-5807G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613005 | ||||||
chrX:47613131 | C | CA | 12 | a0001c0001t0001g0050a0001c0001t0001g0181a0001c0001t0001g0182others(9): Show | 12 | HG00735.hp1 HG01884.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.378-5934dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | ||||||
chrX:47613131 | C | CAA | 1 | a0001c0002t0002g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.378-5935_378-5934d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | ||||||
chrX:47613131 | CA | C | 84 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0049others(81): Show | 87 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378-5934delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | ||||||
chrX:47613131 | CAA | C | 5 | a0001c0002t0001g0013a0001c0002t0001g0018a0001c0002t0001g0232others(2): Show | 5 | HG01891.hp2 HG01943.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-5935_378-5934d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | ||||||
chrX:47613156 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-5958T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613156 | ||||||
chrX:47613181 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-5983C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613181 | ||||||
chrX:47613332 | T | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0015 | 2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.377+6020A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613332 | ||||||
chrX:47613615 | C | T | 4 | a0001c0001t0001g0042a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5737G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613615 | ||||||
chrX:47613736 | C | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(74): Show | 80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+5616G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613736 | ||||||
chrX:47613738 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.377+5614G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613738 | ||||||
chrX:47613766 | T | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0045others(86): Show | 92 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.377+5586A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613766 | ||||||
chrX:47613833 | A | G | 9 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(6): Show | 9 | HG01934.hp1 HG02258.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.377+5519T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613833 | ||||||
chrX:47613875 | G | A | 3 | a0001c0001t0001g0045a0004c0006t0001g0268a0004c0006t0001g0269 | 3 | HG01081.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.377+5477C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613875 | ||||||
chrX:47613914 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.377+5438G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613914 | ||||||
chrX:47613916 | G | T | 4 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0255others(1): Show | 4 | NA18953.hp1 NA19000.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5436C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613916 | ||||||
chrX:47614182 | C | T | 4 | a0001c0001t0001g0042a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5170G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614182 | ||||||
chrX:47614377 | G | C | 1 | a0001c0002t0001g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.377+4975C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614377 | ||||||
chrX:47614412 | T | TG | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.377+4939dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614412 | ||||||
chrX:47614497 | T | C | 63 | a0001c0001t0001g0048a0001c0002t0001g0014a0001c0002t0001g0015others(60): Show | 63 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.377+4855A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614497 | ||||||
chrX:47614572 | C | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(74): Show | 80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+4780G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614572 | ||||||
chrX:47614715 | C | G | 2 | a0001c0002t0001g0218a0001c0002t0001g0219 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.377+4637G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614715 | ||||||
chrX:47614777 | C | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0014a0001c0002t0001g0015others(74): Show | 80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+4575G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614777 | ||||||
chrX:47615243 | A | T | 1 | a0001c0002t0001g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.377+4109T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615243 | ||||||
chrX:47615430 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.377+3922G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615430 | ||||||
chrX:47615891 | C | CA | 1 | a0001c0002t0003g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.377+3460dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615891 | ||||||
chrX:47615891 | CA | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0252 | 2 | NA18987.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.377+3460delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615891 | ||||||
chrX:47615975 | TA | T | 1 | a0001c0002t0001g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.377+3376delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615975 | ||||||
chrX:47616051 | C | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(90): Show | 96 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.377+3301G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616051 | ||||||
chrX:47616210 | C | G | 1 | a0001c0002t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.377+3142G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616210 | ||||||
chrX:47616372 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2980T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616372 | ||||||
chrX:47616373 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2979T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616373 | ||||||
chrX:47616374 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2978T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616374 | ||||||
chrX:47616375 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2977C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616375 | ||||||
chrX:47616376 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2976T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616376 | ||||||
chrX:47616379 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2973T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616379 | ||||||
chrX:47616380 | AATGG | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2968_377+2971d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616380 | ||||||
chrX:47616386 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2966T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616386 | ||||||
chrX:47616391 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2961A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616391 | ||||||
chrX:47616392 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2960A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616392 | ||||||
chrX:47616394 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2958T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616394 | ||||||
chrX:47616395 | ATTTG | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2953_377+2956d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616395 | ||||||
chrX:47616400 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2952A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616400 | ||||||
chrX:47616403 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2949A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616403 | ||||||
chrX:47616404 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2948A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616404 | ||||||
chrX:47616406 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2946A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616406 | ||||||
chrX:47616408 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2944C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616408 | ||||||
chrX:47616413 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2939C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616413 | ||||||
chrX:47616414 | GGA | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2936_377+2937d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616414 | ||||||
chrX:47616419 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2933C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616419 | ||||||
chrX:47616425 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2927C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616425 | ||||||
chrX:47616427 | C | CCT | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2924_377+2925i others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616427 | ||||||
chrX:47616428 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2924T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616428 | ||||||
chrX:47616429 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2923C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616429 | ||||||
chrX:47616431 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2921T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616431 | ||||||
chrX:47616432 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2920A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616432 | ||||||
chrX:47616436 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2916T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616436 | ||||||
chrX:47616438 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2914T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616438 | ||||||
chrX:47616440 | A | T | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2912T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616440 | ||||||
chrX:47616441 | T | TGTTGTTG others(1): Show |
1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2910_377+2911i others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616441 | ||||||
chrX:47616442 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2910T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616442 | ||||||
chrX:47616444 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2908A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616444 | ||||||
chrX:47616446 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2906T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616446 | ||||||
chrX:47616665 | A | G | 1 | a0001c0002t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.377+2687T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616665 | ||||||
chrX:47616973 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.377+2379A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616973 | ||||||
chrX:47617051 | A | G | 2 | a0001c0002t0001g0014a0001c0002t0001g0015 | 2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.377+2301T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617051 | ||||||
chrX:47617414 | T | A | 1 | a0001c0002t0001g0041 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.377+1938A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617414 | ||||||
chrX:47617513 | G | T | 79 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0002t0001g0002others(76): Show | 82 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.377+1839C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617513 | ||||||
chrX:47617842 | G | A | 1 | a0001c0002t0003g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.377+1510C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617842 | ||||||
chrX:47617860 | G | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0189a0001c0001t0001g0190others(23): Show | 27 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.377+1492C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617860 | ||||||
chrX:47617878 | A | T | 4 | a0001c0002t0001g0013a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1474T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617878 | ||||||
chrX:47617966 | G | C | 1 | a0001c0003t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+1386C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617966 | ||||||
chrX:47618022 | T | C | 14 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0002t0001g0253others(11): Show | 14 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+1330A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618022 | ||||||
chrX:47618068 | C | T | 91 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(88): Show | 94 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.377+1284G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618068 | ||||||
chrX:47618269 | G | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0002t0001g0212 | 3 | NA18945.hp1 NA18975.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.377+1083C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618269 | ||||||
chrX:47618690 | C | G | 4 | a0001c0001t0001g0011a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01884.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+662G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618690 | ||||||
chrX:47618702 | G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.377+650C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618702 | ||||||
chrX:47618786 | G | A | 51 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0002t0001g0002others(48): Show | 54 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.377+566C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618786 | ||||||
chrX:47619178 | G | A | 1 | a0001c0002t0001g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.377+174C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47619178 | ||||||
chrX:47619273 | G | A | 1 | a0001c0002t0001g0266 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377+79C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47619273 |