Item | Value |
---|---|
geneid | 492 |
ensemblid | ENSG00000067842.19 |
hgncid | 816 |
symbol | ATP2B3 |
name | ATPase plasma membrane Ca2+ transporting 3 |
refseq_nuc | NM_001001344.3 |
refseq_prot | NP_001001344.1 |
ensembl_nuc | ENST00000263519.5 |
ensembl_prot | ENSP00000263519.4 |
mane_status | MANE Select |
chr | chrX |
start | 153517642 |
end | 153582929 |
strand | + |
ver | v1.2 |
region | chrX:153517642-153582929 |
region5000 | chrX:153512642-153587929 |
regionname0 | ATP2B3_chrX_153517642_153582929 |
regionname5000 | ATP2B3_chrX_153512642_153587929 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001 | 1/1 | 1220 | 257 | 74 | 44 | 101 | 7 | 29 | 74 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0002 | 0/0 | 1220 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0003 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0004 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0005 | 0/0 | 665 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0006 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0007 | 0/0 | 76 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3663 | 119 | 49 | 16 | 35 | 5 | 14 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0002 | 0/1 | 3663 | 109 | 5 | 25 | 63 | 1 | 14 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0003 | 0/0 | 3663 | 12 | 10 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0004 | 1/0 | 3663 | 4 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0005 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0006 | 0/0 | 3663 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0007 | 0/0 | 3663 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0008 | 0/0 | 3661 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0009 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0010 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0011 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0012 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0013 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0014 | 0/0 | 3668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0015 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0016 | 0/0 | 3663 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0017 | 0/0 | 3663 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0018 | 0/0 | 3664 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0019 | 0/0 | 3665 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0020 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0021 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0022 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0023 | 0/0 | 3665 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
c0024 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3114 | 122 | 28 | 22 | 51 | 5 | 15 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0002 | 0/0 | 3112 | 38 | 5 | 9 | 14 | 1 | 9 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0003 | 0/0 | 3115 | 12 | 1 | 5 | 4 | 0 | 2 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0004 | 0/0 | 3112 | 9 | 0 | 0 | 9 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0005 | 0/0 | 3113 | 9 | 7 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0006 | 0/0 | 3113 | 6 | 0 | 2 | 4 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0007 | 0/0 | 3114 | 5 | 5 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0008 | 0/0 | 3115 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0009 | 0/0 | 3112 | 3 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0010 | 0/0 | 3115 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0011 | 0/0 | 3114 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0012 | 0/0 | 3114 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0013 | 0/0 | 3114 | 3 | 1 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0014 | 0/0 | 3114 | 3 | 0 | 1 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0015 | 0/0 | 3113 | 2 | 1 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0016 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0017 | 0/0 | 3114 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0018 | 0/0 | 3115 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0019 | 0/0 | 3112 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0020 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0021 | 0/0 | 3107 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0022 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0023 | 0/0 | 3115 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0024 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0025 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0026 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0027 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0028 | 1/0 | 3112 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0029 | 0/0 | 3110 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0030 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0031 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0032 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0033 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0034 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0035 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0036 | 0/0 | 3118 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0037 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0038 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0039 | 0/0 | 3116 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0040 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0041 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0042 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0043 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0044 | 0/0 | 3114 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0045 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0046 | 0/0 | 3113 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0047 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0048 | 0/0 | 3112 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0049 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0050 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0051 | 0/0 | 3112 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0052 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
t0053 | 0/0 | 3114 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008 | 0/0 | 3661 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0000c0013 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0000c0018 | 0/0 | 3664 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001 | 0/0 | 3663 | 119 | 49 | 16 | 35 | 5 | 14 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002 | 0/1 | 3663 | 109 | 5 | 25 | 63 | 1 | 14 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003 | 0/0 | 3663 | 12 | 10 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0004 | 1/0 | 3663 | 4 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0005 | 0/0 | 3663 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0007 | 0/0 | 3663 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0010 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0011 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0015 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0016 | 0/0 | 3663 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0017 | 0/0 | 3663 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0020 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0021 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0022 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0024 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0002c0006 | 0/0 | 3663 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0003c0009 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0004c0019 | 0/0 | 3665 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0005c0012 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0006c0014 | 0/0 | 3668 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0007c0023 | 0/0 | 3665 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008t0021 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0000c0013t0041 | 0/0 | 6778 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0000c0018t0013 | 0/0 | 6777 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0001 | 0/0 | 6776 | 55 | 22 | 8 | 12 | 4 | 9 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0002 | 0/0 | 6774 | 8 | 3 | 1 | 2 | 1 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0003 | 0/0 | 6777 | 5 | 1 | 3 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0004 | 0/0 | 6774 | 9 | 0 | 0 | 9 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0005 | 0/0 | 6775 | 7 | 5 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0006 | 0/0 | 6775 | 5 | 0 | 2 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0008 | 0/0 | 6777 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0009 | 0/0 | 6774 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0010 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0011 | 0/0 | 6776 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0013 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0014 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0015 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0016 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0018 | 0/0 | 6777 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0019 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0020 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0022 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0027 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0031 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0033 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0035 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0038 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0039 | 0/0 | 6778 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0042 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0046 | 0/0 | 6775 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0049 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0050 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0051 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0001t0053 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0001 | 0/1 | 6776 | 58 | 3 | 14 | 33 | 1 | 6 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0002 | 0/0 | 6774 | 25 | 0 | 6 | 12 | 0 | 7 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0003 | 0/0 | 6777 | 6 | 0 | 2 | 3 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0006 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0010 | 0/0 | 6777 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0012 | 0/0 | 6776 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0013 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0014 | 0/0 | 6776 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0016 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0017 | 0/0 | 6776 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0018 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0029 | 0/0 | 6772 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0030 | 0/0 | 6773 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0032 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0037 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0040 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0043 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0002t0045 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0001 | 0/0 | 6776 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0002 | 0/0 | 6774 | 4 | 2 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0024 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0026 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0034 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0047 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0003t0052 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0004t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0004t0009 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0004t0015 | 0/0 | 6775 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0004t0028 | 1/0 | 6774 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0005t0007 | 0/0 | 6776 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0007t0001 | 0/0 | 6776 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0010t0005 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0011t0023 | 0/0 | 6777 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0015t0001 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0016t0002 | 0/0 | 6774 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0017t0048 | 0/0 | 6774 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0020t0009 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0021t0019 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0022t0025 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0001c0024t0001 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0002c0006t0001 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0002c0006t0003 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0003c0009t0005 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0004c0019t0001 | 0/0 | 6778 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0005c0012t0044 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0006c0014t0036 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
a0007c0023t0001 | 0/0 | 6778 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | copy fasta | chrX | 153512642 | 153587929 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008t0021g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0000c0013t0041g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0000c0018t0013g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0006g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0008g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0015g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0016g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0018g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0020g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0022g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0027g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0031g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0033g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0035g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0038g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0039g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0042g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0046g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0049g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0050g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0051g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0001t0053g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0013g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0014g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0017g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0017g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0018g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0029g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0030g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0032g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0037g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0040g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0043g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0002t0045g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0026g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0034g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0047g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0003t0052g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0004t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0004t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0004t0015g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0004t0028g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0005t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0010t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0011t0023g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0015t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0016t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0017t0048g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0020t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0021t0019g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0022t0025g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0001c0024t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0002c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0002c0006t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0003c0009t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0004c0019t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0005c0012t0044g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0006c0014t0036g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
a0007c0023t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00280 | hp1 | a0001 | c0017 | t0048 | g0049 | EUR | FIN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00639 | hp2 | a0001 | c0002 | t0017 | g0201 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0236 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00741 | hp1 | a0001 | c0001 | t0046 | g0243 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01243 | hp1 | a0001 | c0004 | t0015 | g0225 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01256 | hp1 | a0001 | c0002 | t0017 | g0103 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01433 | hp1 | a0001 | c0002 | t0014 | g0012 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0237 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0211 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02055 | hp1 | a0001 | c0010 | t0005 | g0173 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02056 | hp1 | a0002 | c0006 | t0001 | g0151 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02080 | hp1 | a0001 | c0001 | t0014 | g0064 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02080 | hp2 | a0002 | c0006 | t0003 | g0140 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02135 | hp1 | a0001 | c0001 | t0031 | g0057 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0227 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CDX | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02257 | hp1 | a0001 | c0001 | t0053 | g0084 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02257 | hp2 | a0001 | c0003 | t0007 | g0231 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02280 | hp1 | a0001 | c0004 | t0007 | g0226 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02451 | hp1 | a0001 | c0003 | t0047 | g0100 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02451 | hp2 | a0001 | c0001 | t0049 | g0083 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02615 | hp1 | a0001 | c0021 | t0019 | g0075 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02622 | hp1 | a0001 | c0001 | t0016 | g0186 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0037 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02717 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02809 | hp1 | a0001 | c0011 | t0023 | g0232 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02809 | hp2 | a0001 | c0004 | t0009 | g0239 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02818 | hp1 | a0001 | c0001 | t0019 | g0207 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02886 | hp2 | a0001 | c0003 | t0034 | g0029 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02922 | hp1 | a0001 | c0001 | t0051 | g0017 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02970 | hp1 | a0001 | c0003 | t0026 | g0235 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02976 | hp1 | a0001 | c0003 | t0024 | g0238 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02976 | hp2 | a0000 | c0008 | t0021 | g0228 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03041 | hp2 | a0003 | c0009 | t0005 | g0081 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03195 | hp2 | a0001 | c0015 | t0001 | g0152 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03453 | hp1 | a0001 | c0005 | t0007 | g0016 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03453 | hp2 | a0001 | c0001 | t0020 | g0230 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03486 | hp1 | a0001 | c0002 | t0016 | g0076 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03486 | hp2 | a0001 | c0003 | t0052 | g0101 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0096 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0032 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03654 | hp1 | a0001 | c0001 | t0039 | g0056 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03831 | hp1 | a0001 | c0016 | t0002 | g0198 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03834 | hp2 | a0001 | c0001 | t0005 | g0091 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03927 | hp1 | a0000 | c0018 | t0013 | g0090 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04115 | hp1 | a0001 | c0001 | t0018 | g0052 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18906 | hp1 | a0001 | c0005 | t0007 | g0016 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18939 | hp2 | a0001 | c0002 | t0013 | g0241 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18943 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18944 | hp1 | a0001 | c0007 | t0001 | g0069 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18948 | hp1 | a0001 | c0002 | t0012 | g0087 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18950 | hp2 | a0001 | c0002 | t0014 | g0099 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18960 | hp1 | a0001 | c0002 | t0043 | g0106 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18961 | hp1 | a0001 | c0002 | t0010 | g0102 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18962 | hp1 | a0007 | c0023 | t0001 | g0097 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18966 | hp1 | a0001 | c0024 | t0001 | g0183 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18975 | hp1 | a0001 | c0001 | t0033 | g0214 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18982 | hp1 | a0006 | c0014 | t0036 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18985 | hp1 | a0005 | c0012 | t0044 | g0224 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18995 | hp1 | a0001 | c0001 | t0038 | g0007 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18998 | hp1 | a0001 | c0002 | t0012 | g0088 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA18998 | hp2 | a0001 | c0001 | t0035 | g0070 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19000 | hp1 | a0001 | c0002 | t0010 | g0142 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19005 | hp1 | a0001 | c0002 | t0012 | g0089 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19010 | hp1 | a0001 | c0002 | t0037 | g0073 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19011 | hp2 | a0001 | c0002 | t0018 | g0172 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0085 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19043 | hp1 | a0001 | c0022 | t0025 | g0234 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19057 | hp1 | a0001 | c0002 | t0032 | g0105 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19057 | hp2 | a0001 | c0001 | t0050 | g0107 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19063 | hp1 | a0001 | c0002 | t0030 | g0018 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19067 | hp1 | a0001 | c0002 | t0045 | g0157 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19068 | hp1 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19077 | hp2 | a0004 | c0019 | t0001 | g0114 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19080 | hp1 | a0001 | c0007 | t0001 | g0046 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19082 | hp1 | a0001 | c0001 | t0042 | g0220 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19083 | hp1 | a0000 | c0013 | t0041 | g0041 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19084 | hp2 | a0001 | c0002 | t0029 | g0019 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | ASW | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ASW | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | TSI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | GIH | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0166 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02109 | hp2 | a0001 | c0020 | t0009 | g0229 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02486 | hp1 | a0001 | c0001 | t0027 | g0240 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02559 | hp1 | a0001 | c0002 | t0040 | g0068 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0233 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0165 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0159 | REF | REF | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0028 | g0205 | REF | REF | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
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:153518431
|
GGA | G | 1 | a0001 | 1 | NA19084.hp2 | splice_region_variant | LOW | c.-246_-245delGA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | chrX | 153518431 | ||||||
chrX:153541373
|
A | AC | 1 | a0007 | 1 | NA18962.hp1 | frameshift_variant | HIGH | c.225dupC | p.Asn76fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/22 | 706/6774 | 226/3663 | 76/1220 | INFO_REALIGN_3_PRIME | chrX | 153541373 | |
chrX:153541419
|
TC | T | 1 | a0007 | 1 | NA18962.hp1 | frameshift_variant | HIGH | c.275delC | p.Pro92fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/22 | 755/6774 | 275/3663 | 92/1220 | INFO_REALIGN_3_PRIME | chrX | 153541419 | |
chrX:153541436
|
A | AAACC | 1 | a0007 | 1 | NA18962.hp1 | frameshift_variant | HIGH | c.287_288insACCA | p.Thr97fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/22 | 768/6774 | 288/3663 | 96/1220 | INFO_REALIGN_3_PRIME | chrX | 153541436 | |
chrX:153541825
|
G | A | 1 | a0003 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Gln | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1043/6774 | 563/3663 | 188/1220 | chrX | 153541825 | ||
chrX:153541900
|
TG | T | 1 | a0007 | 1 | NA18962.hp1 | frameshift_variant | HIGH | c.643delG | p.Asp215fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1123/6774 | 643/3663 | 215/1220 | INFO_REALIGN_3_PRIME | chrX | 153541900 | |
chrX:153541915
|
AG | A | 1 | a0007 | 1 | NA18962.hp1 | frameshift_variant | HIGH | c.655delG | p.Val219fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1135/6774 | 655/3663 | 219/1220 | INFO_REALIGN_3_PRIME | chrX | 153541915 | |
chrX:153550143
|
C | CGT | 1 | a0004 | 1 | NA19077.hp2 | frameshift_variant | HIGH | c.1682_1683dupTG | p.Arg562fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/22 | 2164/6774 | 1684/3663 | 562/1220 | INFO_REALIGN_3_PRIME | chrX | 153550143 | |
chrX:153550226
|
G | A | 1 | a0002 | 2 | HG02056.hp1 HG02080.hp2 |
missense_variant | MODERATE | c.1763G>A | p.Arg588His | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/22 | 2243/6774 | 1763/3663 | 588/1220 | chrX | 153550226 | ||
chrX:153553088
|
A | AC | 1 | a0005 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.1879dupC | p.Arg627fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/22 | 2360/6774 | 1880/3663 | 627/1220 | INFO_REALIGN_3_PRIME | chrX | 153553088 | |
chrX:153580055
|
C | CTTCAT | 1 | a0006 | 1 | NA18982.hp1 | frameshift_variant | HIGH | c.3421_3425dupTTCAT | p.Met1142fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3906/6774 | 3426/3663 | 1142/1220 | INFO_REALIGN_3_PRIME | chrX | 153580055 | |
chrX:153580102
|
TC | T | 1 | a0000 | 1 | HG02976.hp2 | frameshift_variant | HIGH | c.3470delC | p.Pro1157fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3950/6774 | 3470/3663 | 1157/1220 | INFO_REALIGN_3_PRIME | chrX | 153580102 | |
chrX:153580149
|
CG | C | 1 | a0000 | 1 | HG02976.hp2 | frameshift_variant | HIGH | c.3517delG | p.Ala1173fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3997/6774 | 3517/3663 | 1173/1220 | INFO_REALIGN_3_PRIME | chrX | 153580149 | |
chrX:153580152
|
G | GC | 1 | a0000 | 2 | HG03927.hp1 NA19083.hp1 |
frameshift_variant | HIGH | c.3524dupC | p.Pro1176fs | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 4005/6774 | 3525/3663 | 1175/1220 | INFO_REALIGN_3_PRIME | chrX | 153580152 |
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:153536406
|
C | T | 1 | a0001c0024 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.159C>T | p.Tyr53Tyr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/22 | 639/6774 | 159/3663 | 53/1220 | chrX | 153536406 | ||
chrX:153541480
|
C | A | 1 | a0000c0008 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.330C>A | p.Thr110Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/22 | 810/6774 | 330/3663 | 110/1220 | chrX | 153541480 | ||
chrX:153541892
|
G | A | 1 | a0001c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.630G>A | p.Ala210Ala | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1110/6774 | 630/3663 | 210/1220 | chrX | 153541892 | ||
chrX:153543083
|
C | T | 1 | a0001c0022 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.831C>T | p.Thr277Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/22 | 1311/6774 | 831/3663 | 277/1220 | chrX | 153543083 | ||
chrX:153548740
|
G | A | 1 | a0001c0005 | 2 | HG03453.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1224G>A | p.Pro408Pro | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/22 | 1704/6774 | 1224/3663 | 408/1220 | chrX | 153548740 | ||
chrX:153548809
|
G | A | 2 | a0000c0008a0001c0011 | 2 | HG02809.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.1293G>A | p.Glu431Glu | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/22 | 1773/6774 | 1293/3663 | 431/1220 | chrX | 153548809 | ||
chrX:153549631
|
A | G | 23 | a0000c0008a0000c0013a0000c0018others(20): Show | 263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
synonymous_variant | LOW | c.1473A>G | p.Gly491Gly | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 11/22 | 1953/6774 | 1473/3663 | 491/1220 | chrX | 153549631 | ||
chrX:153550098
|
C | T | 2 | a0001c0020a0001c0021 | 2 | HG02109.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.1635C>T | p.Cys545Cys | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/22 | 2115/6774 | 1635/3663 | 545/1220 | chrX | 153550098 | ||
chrX:153556123
|
G | A | 1 | a0001c0020 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2133G>A | p.Thr711Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/22 | 2613/6774 | 2133/3663 | 711/1220 | chrX | 153556123 | ||
chrX:153558270
|
G | C | 9 | a0000c0013a0001c0002a0001c0015others(6): Show | 118 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(115): Show |
synonymous_variant | LOW | c.2592G>C | p.Val864Val | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/22 | 3072/6774 | 2592/3663 | 864/1220 | chrX | 153558270 | ||
chrX:153558273
|
C | T | 1 | a0001c0016 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2595C>T | p.Ile865Ile | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/22 | 3075/6774 | 2595/3663 | 865/1220 | chrX | 153558273 | ||
chrX:153560878
|
C | T | 1 | a0001c0015 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3042C>T | p.Phe1014Phe | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/22 | 3522/6774 | 3042/3663 | 1014/1220 | chrX | 153560878 | ||
chrX:153565037
|
T | C | 5 | a0000c0008a0001c0003a0001c0010others(2): Show | 16 | HG01361.hp2 HG01934.hp1 HG02055.hp1 others(13): Show |
synonymous_variant | LOW | c.3276T>C | p.His1092His | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/22 | 3756/6774 | 3276/3663 | 1092/1220 | chrX | 153565037 | ||
chrX:153580007
|
G | A | 1 | a0001c0017 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.3372G>A | p.Ser1124Ser | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3852/6774 | 3372/3663 | 1124/1220 | chrX | 153580007 | ||
chrX:153580106
|
G | A | 1 | a0001c0007 | 2 | NA18944.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3471G>A | p.Pro1157Pro | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3951/6774 | 3471/3663 | 1157/1220 | chrX | 153580106 |
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:153517683
|
C | G | 64 | a0000c0013t0041a0000c0018t0013a0001c0001t0001others(61): Show | 248 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(245): Show |
5_prime_UTR_variant | MODIFIER | c.-439C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/22 | 18565 | chrX | 153517683 | |||||
chrX:153517722
|
C | T | 64 | a0000c0013t0041a0000c0018t0013a0001c0001t0001others(61): Show | 248 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(245): Show |
5_prime_UTR_variant | MODIFIER | c.-400C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/22 | 18526 | chrX | 153517722 | |||||
chrX:153518435
|
C | A | 1 | a0001c0002t0029 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | 17813 | chrX | 153518435 | |||||
chrX:153518436
|
G | A | 17 | a0000c0008t0021a0001c0001t0007a0001c0001t0009others(14): Show | 18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-242G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | 17812 | chrX | 153518436 | |||||
chrX:153518465
|
CT | C | 1 | a0001c0002t0030 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-211delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | 17781 | INFO_REALIGN_3_PRIME | chrX | 153518465 | ||||
chrX:153580328
|
G | A | 1 | a0001c0001t0020 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 30 | chrX | 153580328 | |||||
chrX:153580399
|
C | CA | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 106 | INFO_REALIGN_3_PRIME | chrX | 153580399 | ||||
chrX:153580405
|
G | A | 1 | a0001c0001t0031 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 107 | chrX | 153580405 | |||||
chrX:153580406
|
AG | A | 1 | a0001c0002t0032 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*111delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 111 | INFO_REALIGN_3_PRIME | chrX | 153580406 | ||||
chrX:153580728
|
A | T | 2 | a0001c0001t0053a0001c0003t0052 | 2 | HG02257.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 430 | chrX | 153580728 | |||||
chrX:153580781
|
C | CA | 44 | a0000c0013t0041a0001c0001t0001a0001c0001t0003others(41): Show | 187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*498dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 499 | INFO_REALIGN_3_PRIME | chrX | 153580781 | ||||
chrX:153580781
|
C | CAA | 6 | a0001c0001t0010a0001c0001t0016a0001c0001t0022others(3): Show | 7 | HG00544.hp2 HG02622.hp1 HG03486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*498dupAA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 499 | INFO_REALIGN_3_PRIME | chrX | 153580781 | ||||
chrX:153580781
|
CA | C | 1 | a0001c0001t0051 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 498 | INFO_REALIGN_3_PRIME | chrX | 153580781 | ||||
chrX:153580851
|
C | T | 2 | a0001c0002t0012a0001c0002t0045 | 4 | NA18948.hp1 NA18998.hp1 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*553C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 553 | chrX | 153580851 | |||||
chrX:153580965
|
G | A | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 667 | chrX | 153580965 | |||||
chrX:153581083
|
T | A | 1 | a0001c0001t0046 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 785 | chrX | 153581083 | |||||
chrX:153581084
|
G | GT | 5 | a0001c0001t0014a0001c0001t0027a0001c0001t0050others(2): Show | 6 | HG01433.hp1 HG02080.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*801dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 802 | INFO_REALIGN_3_PRIME | chrX | 153581084 | ||||
chrX:153581084
|
GT | G | 3 | a0001c0001t0004a0001c0001t0033a0001c0002t0040 | 11 | HG02559.hp1 NA18612.hp1 NA18939.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*801delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 801 | INFO_REALIGN_3_PRIME | chrX | 153581084 | ||||
chrX:153581085
|
T | TTG | 3 | a0001c0001t0018a0001c0001t0039a0001c0002t0018 | 3 | HG03654.hp1 HG04115.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*788_*789insGT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 789 | INFO_REALIGN_3_PRIME | chrX | 153581085 | ||||
chrX:153581086
|
T | TG | 49 | a0000c0018t0013a0001c0001t0001a0001c0001t0003others(46): Show | 187 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*789insG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 789 | chrX | 153581086 | |||||
chrX:153581166
|
A | G | 2 | a0001c0001t0019a0001c0021t0019 | 2 | HG02615.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 868 | chrX | 153581166 | |||||
chrX:153581173
|
G | A | 1 | a0001c0003t0034 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 875 | chrX | 153581173 | |||||
chrX:153581191
|
G | GC | 1 | a0000c0013t0041 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 897 | INFO_REALIGN_3_PRIME | chrX | 153581191 | ||||
chrX:153581220
|
G | A | 1 | a0001c0003t0052 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*922G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 922 | chrX | 153581220 | |||||
chrX:153581304
|
G | T | 4 | a0000c0008t0021a0001c0001t0027a0001c0001t0049others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1006G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1006 | chrX | 153581304 | |||||
chrX:153581309
|
AT | A | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1015delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1015 | INFO_REALIGN_3_PRIME | chrX | 153581309 | ||||
chrX:153581324
|
G | GA | 2 | a0001c0001t0035a0006c0014t0036 | 2 | NA18982.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1033 | INFO_REALIGN_3_PRIME | chrX | 153581324 | ||||
chrX:153581369
|
AG | A | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1075 | INFO_REALIGN_3_PRIME | chrX | 153581369 | ||||
chrX:153581434
|
GC | G | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1141delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1141 | INFO_REALIGN_3_PRIME | chrX | 153581434 | ||||
chrX:153581470
|
T | C | 1 | a0001c0001t0011 | 3 | HG02630.hp2 HG02717.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1172T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1172 | chrX | 153581470 | |||||
chrX:153581521
|
A | AG | 1 | a0006c0014t0036 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1229 | INFO_REALIGN_3_PRIME | chrX | 153581521 | ||||
chrX:153581563
|
AG | A | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1268 | INFO_REALIGN_3_PRIME | chrX | 153581563 | ||||
chrX:153581614
|
G | T | 1 | a0001c0002t0017 | 2 | HG00639.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1316G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1316 | chrX | 153581614 | |||||
chrX:153581672
|
G | C | 2 | a0001c0001t0011a0001c0003t0052 | 4 | HG02630.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1374G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1374 | chrX | 153581672 | |||||
chrX:153581779
|
C | A | 1 | a0001c0017t0048 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1481 | chrX | 153581779 | |||||
chrX:153581833
|
T | C | 58 | a0000c0018t0013a0001c0001t0001a0001c0001t0003others(55): Show | 204 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1535 | chrX | 153581833 | |||||
chrX:153581843
|
G | C | 59 | a0000c0008t0021a0000c0018t0013a0001c0001t0001others(56): Show | 205 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1545G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1545 | chrX | 153581843 | |||||
chrX:153581943
|
GC | G | 1 | a0001c0001t0038 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1649 | INFO_REALIGN_3_PRIME | chrX | 153581943 | ||||
chrX:153581973
|
G | GT | 1 | a0006c0014t0036 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675_*1676insT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1676 | chrX | 153581973 | |||||
chrX:153582005
|
G | A | 4 | a0001c0001t0004a0001c0001t0033a0001c0001t0042others(1): Show | 12 | HG02559.hp1 NA18612.hp1 NA18939.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1707G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1707 | chrX | 153582005 | |||||
chrX:153582030
|
T | G | 59 | a0000c0008t0021a0000c0018t0013a0001c0001t0001others(56): Show | 205 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1732T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1732 | chrX | 153582030 | |||||
chrX:153582076
|
C | T | 1 | a0001c0022t0025 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1778 | chrX | 153582076 | |||||
chrX:153582095
|
G | T | 1 | a0001c0001t0046 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1797G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1797 | chrX | 153582095 | |||||
chrX:153582197
|
AC | A | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1903delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1903 | INFO_REALIGN_3_PRIME | chrX | 153582197 | ||||
chrX:153582253
|
A | G | 1 | a0001c0001t0020 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1955 | chrX | 153582253 | |||||
chrX:153582357
|
G | GT | 1 | a0006c0014t0036 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2062dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2063 | INFO_REALIGN_3_PRIME | chrX | 153582357 | ||||
chrX:153582432
|
G | A | 1 | a0001c0002t0037 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2134 | chrX | 153582432 | |||||
chrX:153582540
|
C | T | 1 | a0001c0003t0024 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2242C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2242 | chrX | 153582540 | |||||
chrX:153582628
|
C | CG | 15 | a0000c0013t0041a0000c0018t0013a0001c0001t0003others(12): Show | 25 | HG00735.hp1 HG00735.hp2 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2335 | INFO_REALIGN_3_PRIME | chrX | 153582628 | ||||
chrX:153582660
|
G | GT | 1 | a0006c0014t0036 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2368 | INFO_REALIGN_3_PRIME | chrX | 153582660 | ||||
chrX:153582703
|
GC | G | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2409delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2409 | INFO_REALIGN_3_PRIME | chrX | 153582703 | ||||
chrX:153582899
|
T | TA | 4 | a0001c0001t0008a0001c0001t0016a0001c0001t0022others(1): Show | 7 | HG02280.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2610dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2611 | INFO_REALIGN_3_PRIME | chrX | 153582899 | ||||
chrX:153582899
|
TA | T | 1 | a0006c0014t0036 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2610delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2610 | INFO_REALIGN_3_PRIME | chrX | 153582899 | ||||
chrX:153582904
|
A | C | 1 | a0000c0008t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2606A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2606 | chrX | 153582904 |
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:153517893
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0046g0243a0001c0002t0001g0242 | 3 | HG00609.hp1 HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-247+18C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153517893 | ||||||
chrX:153517912
|
T | TG | 1 | a0001c0002t0013g0241 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-247+40dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153517912 | |||||
chrX:153517935
|
CA | C | 17 | a0000c0008t0021g0228a0001c0001t0007g0237a0001c0001t0009g0236others(14): Show | 18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-247+62delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153517935 | |||||
chrX:153517982
|
G | A | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-247+107G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153517982 | ||||||
chrX:153518081
|
AG | A | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-247+208delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518081 | |||||
chrX:153518152
|
A | AG | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-246-278dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518152 | |||||
chrX:153518166
|
T | TG | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-246-261dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518166 | |||||
chrX:153518188
|
A | AG | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-246-241dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518188 | |||||
chrX:153518271
|
T | TC | 2 | a0001c0001t0002g0039a0001c0001t0004g0040 | 2 | NA18939.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-246-154dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518271 | |||||
chrX:153518278
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 26 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.-246-154C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153518278 | ||||||
chrX:153518304
|
C | T | 2 | a0001c0001t0011g0037a0001c0001t0011g0038 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-246-128C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153518304 | ||||||
chrX:153518347
|
G | GC | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-246-82dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518347 | |||||
chrX:153518356
|
AC | A | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-246-72delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518356 | |||||
chrX:153518396
|
CG | C | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-246-32delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518396 | |||||
chrX:153518427
|
TC | T | 2 | a0001c0002t0029g0019a0001c0002t0030g0018 | 2 | NA19063.hp1 NA19084.hp2 |
splice_region_variant&intron_variant | LOW | c.-246-3delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153518427 | |||||
chrX:153518556
|
G | C | 17 | a0000c0008t0021g0228a0001c0001t0007g0237a0001c0001t0009g0236others(14): Show | 18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.-127+5G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153518556 | ||||||
chrX:153518678
|
AG | A | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-127+131delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153518678 | |||||
chrX:153518691
|
CG | C | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+144delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153518691 | |||||
chrX:153518995
|
G | A | 2 | a0001c0001t0001g0042a0001c0002t0002g0043 | 2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-127+444G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153518995 | ||||||
chrX:153519022
|
A | ACCT | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+477_-127+479d others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519022 | |||||
chrX:153519070
|
C | T | 13 | a0001c0001t0001g0217a0001c0001t0004g0014a0001c0001t0004g0040others(10): Show | 15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-127+519C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519070 | ||||||
chrX:153519106
|
A | AC | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+555_-127+556i others(3): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519106 | ||||||
chrX:153519138
|
CA | C | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+588delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519138 | ||||||
chrX:153519263
|
GC | G | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-127+717delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519263 | |||||
chrX:153519287
|
GC | G | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-127+739delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519287 | |||||
chrX:153519326
|
AG | A | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+778delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519326 | |||||
chrX:153519397
|
C | T | 1 | a0001c0001t0011g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-127+846C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519397 | ||||||
chrX:153519417
|
A | AG | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+867dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519417 | |||||
chrX:153519502
|
G | A | 3 | a0001c0001t0015g0227a0001c0004t0007g0226a0001c0004t0015g0225 | 3 | HG01243.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-127+951G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519502 | ||||||
chrX:153519530
|
TG | T | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+982delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519530 | |||||
chrX:153519695
|
C | CG | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-127+1149dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519695 | |||||
chrX:153519696
|
G | A | 3 | a0001c0001t0001g0042a0001c0002t0002g0043a0001c0002t0002g0044 | 3 | HG02735.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-127+1145G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519696 | ||||||
chrX:153519721
|
T | TC | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1171dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519721 | |||||
chrX:153519741
|
GC | G | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1192delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519741 | |||||
chrX:153519764
|
GT | G | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1216delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519764 | |||||
chrX:153519799
|
A | AAG | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1248_-127+124 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519799 | ||||||
chrX:153519804
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1253G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519804 | ||||||
chrX:153519853
|
G | A | 226 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(223): Show | 242 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-127+1302G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519853 | ||||||
chrX:153519861
|
G | A | 1 | a0001c0007t0001g0046 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-127+1310G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519861 | ||||||
chrX:153519866
|
GC | G | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1317delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519866 | |||||
chrX:153519886
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-127+1335G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519886 | ||||||
chrX:153519950
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(79): Show | 90 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-127+1399G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519950 | ||||||
chrX:153519962
|
G | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+1411G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519962 | ||||||
chrX:153519990
|
A | AG | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-127+1442dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519990 | |||||
chrX:153519990
|
AG | A | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1442delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153519990 | |||||
chrX:153520045
|
TG | T | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1496delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520045 | |||||
chrX:153520108
|
C | T | 1 | a0001c0001t0027g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-127+1557C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520108 | ||||||
chrX:153520138
|
G | C | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-127+1587G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520138 | ||||||
chrX:153520218
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+1667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520218 | ||||||
chrX:153520232
|
A | G | 20 | a0001c0001t0001g0042a0001c0001t0016g0186a0001c0002t0001g0190others(17): Show | 22 | HG00423.hp2 HG00544.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-127+1681A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520232 | ||||||
chrX:153520314
|
CT | C | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1765delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520314 | |||||
chrX:153520369
|
C | T | 8 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(5): Show | 9 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+1818C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520369 | ||||||
chrX:153520430
|
CT | C | 1 | a0001c0001t0001g0020 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-127+1880delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520430 | ||||||
chrX:153520431
|
T | TC | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1884dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520431 | |||||
chrX:153520431
|
TC | T | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1884delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520431 | |||||
chrX:153520440
|
AT | A | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1893delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520440 | |||||
chrX:153520459
|
T | A | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1908T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520459 | ||||||
chrX:153520491
|
TG | T | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1942delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520491 | |||||
chrX:153520830
|
T | C | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-127+2279T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520830 | ||||||
chrX:153520864
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-127+2313C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520864 | ||||||
chrX:153520864
|
CG | C | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+2317delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153520864 | |||||
chrX:153520880
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-127+2329G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520880 | ||||||
chrX:153520917
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-127+2366G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520917 | ||||||
chrX:153521006
|
G | GC | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+2459dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521006 | |||||
chrX:153521196
|
C | CT | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+2647dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521196 | |||||
chrX:153521203
|
A | G | 225 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0002others(222): Show | 242 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-127+2652A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521203 | ||||||
chrX:153521247
|
G | A | 3 | a0001c0002t0012g0087a0001c0002t0012g0088a0001c0002t0012g0089 | 3 | NA18948.hp1 NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-127+2696G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521247 | ||||||
chrX:153521337
|
G | A | 2 | a0000c0018t0013g0090a0001c0001t0005g0091 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-127+2786G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521337 | ||||||
chrX:153521404
|
T | C | 1 | a0001c0001t0019g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-127+2853T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521404 | ||||||
chrX:153521422
|
CA | C | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+2873delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521422 | |||||
chrX:153521474
|
A | AG | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+2926dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521474 | |||||
chrX:153521538
|
GT | G | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+2990delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521538 | |||||
chrX:153521715
|
A | G | 226 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0002others(223): Show | 243 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.-127+3164A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521715 | ||||||
chrX:153521802
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-127+3251G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521802 | ||||||
chrX:153521925
|
G | A | 1 | a0001c0001t0005g0092 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-127+3374G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521925 | ||||||
chrX:153521928
|
C | A | 1 | a0001c0021t0019g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-127+3377C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521928 | ||||||
chrX:153521940
|
TC | T | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+3392delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521940 | |||||
chrX:153521959
|
TG | T | 1 | a0001c0002t0003g0093 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-127+3410delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153521959 | |||||
chrX:153522028
|
G | A | 7 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(4): Show | 8 | HG01934.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+3477G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522028 | ||||||
chrX:153522152
|
T | TG | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+3602dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522152 | |||||
chrX:153522227
|
A | AC | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+3677dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522227 | |||||
chrX:153522380
|
C | A | 18 | a0000c0008t0021g0228a0001c0001t0001g0206a0001c0001t0001g0208others(15): Show | 19 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-127+3829C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522380 | ||||||
chrX:153522380
|
CG | C | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+3832delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522380 | |||||
chrX:153522381
|
G | A | 2 | a0001c0001t0011g0037a0001c0001t0011g0038 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-127+3830G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522381 | ||||||
chrX:153522412
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-127+3861G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522412 | ||||||
chrX:153522445
|
T | TC | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+3898dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522445 | |||||
chrX:153522569
|
G | A | 1 | a0001c0004t0015g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-127+4018G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522569 | ||||||
chrX:153522595
|
C | CA | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-127+4045dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522595 | |||||
chrX:153522596
|
A | AC | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+4051dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522596 | |||||
chrX:153522608
|
GC | G | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-127+4060delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522608 | |||||
chrX:153522737
|
TG | T | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+4191delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522737 | |||||
chrX:153522866
|
G | GC | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+4316dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522866 | |||||
chrX:153522895
|
GT | G | 237 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(234): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-127+4357delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522895 | |||||
chrX:153522895
|
GTT | G | 1 | a0001c0001t0001g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-127+4356_-127+435 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522895 | |||||
chrX:153523022
|
TC | T | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-127+4473delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523022 | |||||
chrX:153523212
|
A | C | 3 | a0001c0001t0049g0083a0001c0001t0053g0084a0001c0003t0002g0085 | 3 | HG02257.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-127+4661A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523212 | ||||||
chrX:153523273
|
G | C | 20 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(17): Show | 22 | HG01884.hp1 HG02040.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.-127+4722G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523273 | ||||||
chrX:153523292
|
CG | C | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+4743delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523292 | |||||
chrX:153523294
|
G | A | 1 | a0001c0001t0016g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127+4743G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523294 | ||||||
chrX:153523295
|
C | A | 1 | a0001c0001t0016g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127+4744C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523295 | ||||||
chrX:153523299
|
C | G | 4 | a0001c0001t0003g0212a0001c0001t0008g0013a0001c0001t0019g0207others(1): Show | 5 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+4748C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523299 | ||||||
chrX:153523352
|
C | T | 1 | a0001c0001t0011g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-127+4801C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523352 | ||||||
chrX:153523354
|
CT | C | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+4805delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523354 | |||||
chrX:153523433
|
C | G | 4 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+4882C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523433 | ||||||
chrX:153523545
|
AT | A | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+4998delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523545 | |||||
chrX:153523688
|
A | AT | 2 | a0001c0002t0001g0181a0001c0004t0015g0225 | 2 | HG00408.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-127+5160dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523688 | |||||
chrX:153523709
|
TTTC | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 80 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-127+5159_-127+516 others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523709 | ||||||
chrX:153523710
|
TTC | T | 19 | a0001c0001t0002g0039a0001c0001t0004g0223a0001c0001t0006g0008others(16): Show | 20 | HG00408.hp2 HG01192.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-127+5160_-127+516 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523710 | ||||||
chrX:153523711
|
TC | T | 128 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(125): Show | 136 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-127+5163delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523711 | |||||
chrX:153523712
|
C | T | 29 | a0000c0008t0021g0228a0001c0001t0001g0175a0001c0001t0001g0176others(26): Show | 30 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.-127+5161C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523712 | ||||||
chrX:153523759
|
G | A | 21 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(18): Show | 23 | HG01884.hp1 HG02040.hp1 HG02129.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+5208G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523759 | ||||||
chrX:153523850
|
C | A | 3 | a0001c0001t0051g0017a0001c0003t0047g0100a0001c0010t0005g0173 | 3 | HG02055.hp1 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-127+5299C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523850 | ||||||
chrX:153523857
|
G | A | 2 | a0001c0001t0020g0230a0001c0020t0009g0229 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-127+5306G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523857 | ||||||
chrX:153524028
|
GA | G | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+5483delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524028 | |||||
chrX:153524066
|
A | G | 4 | a0001c0001t0015g0227a0001c0004t0007g0226a0001c0004t0009g0239others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+5515A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524066 | ||||||
chrX:153524091
|
AT | A | 100 | a0000c0008t0021g0228a0001c0001t0001g0003a0001c0001t0001g0025others(97): Show | 106 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-127+5551delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524091 | |||||
chrX:153524091
|
ATT | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 23 | HG00609.hp1 HG00741.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+5550_-127+555 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524091 | |||||
chrX:153524091
|
ATTT | A | 2 | a0001c0001t0011g0037a0001c0001t0011g0038 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-127+5549_-127+555 others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524091 | |||||
chrX:153524120
|
C | CT | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+5572dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524120 | |||||
chrX:153524238
|
C | CTG | 12 | a0001c0001t0001g0244a0001c0001t0003g0212a0001c0001t0046g0243others(9): Show | 12 | HG00609.hp1 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-127+5707_-127+570 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | |||||
chrX:153524238
|
C | CTGTG | 1 | a0001c0002t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-127+5705_-127+570 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | |||||
chrX:153524238
|
C | CTGTGTGT others(1): Show |
1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-127+5701_-127+570 others(12): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | |||||
chrX:153524238
|
CTG | C | 7 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(4): Show | 8 | HG01934.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+5707_-127+570 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | |||||
chrX:153524238
|
CTGTGTG | C | 1 | a0001c0017t0048g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-127+5703_-127+570 others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | |||||
chrX:153524291
|
C | T | 9 | a0000c0008t0021g0228a0001c0001t0007g0237a0001c0001t0009g0236others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+5740C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524291 | ||||||
chrX:153524320
|
C | CT | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-127+5774dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524320 | |||||
chrX:153524370
|
C | T | 1 | a0001c0003t0052g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-127+5819C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524370 | ||||||
chrX:153524378
|
C | A | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+5827C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524378 | ||||||
chrX:153524395
|
C | T | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+5844C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524395 | ||||||
chrX:153524536
|
A | G | 1 | a0001c0002t0002g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-127+5985A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524536 | ||||||
chrX:153524729
|
G | C | 135 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(132): Show | 143 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-127+6178G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524729 | ||||||
chrX:153524734
|
G | A | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+6183G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524734 | ||||||
chrX:153525025
|
C | CA | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+6475dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525025 | |||||
chrX:153525287
|
C | T | 1 | a0001c0002t0002g0180 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-127+6736C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525287 | ||||||
chrX:153525306
|
G | A | 133 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(130): Show | 141 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-127+6755G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525306 | ||||||
chrX:153525325
|
C | A | 5 | a0001c0001t0001g0244a0001c0001t0046g0243a0001c0002t0001g0242others(2): Show | 5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+6774C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525325 | ||||||
chrX:153525348
|
G | T | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+6797G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525348 | ||||||
chrX:153525378
|
A | AG | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-127+6831dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525378 | |||||
chrX:153525444
|
A | G | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-127+6893A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525444 | ||||||
chrX:153525473
|
C | CT | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+6922_-127+692 others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525473 | ||||||
chrX:153525525
|
G | A | 20 | a0000c0008t0021g0228a0001c0001t0001g0202a0001c0001t0001g0203others(17): Show | 20 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-127+6974G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525525 | ||||||
chrX:153525551
|
G | A | 9 | a0001c0001t0007g0237a0001c0001t0009g0236a0001c0001t0011g0036others(6): Show | 9 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127+7000G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525551 | ||||||
chrX:153525556
|
C | A | 3 | a0001c0001t0051g0017a0001c0003t0047g0100a0001c0010t0005g0173 | 3 | HG02055.hp1 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-127+7005C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525556 | ||||||
chrX:153525563
|
A | G | 25 | a0001c0001t0001g0042a0001c0002t0001g0171a0001c0002t0001g0190others(22): Show | 27 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-127+7012A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525563 | ||||||
chrX:153525641
|
C | CT | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7091dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525641 | |||||
chrX:153525693
|
TG | T | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+7144delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525693 | |||||
chrX:153525754
|
C | T | 1 | a0001c0003t0002g0211 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-127+7203C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525754 | ||||||
chrX:153525802
|
C | T | 13 | a0001c0001t0001g0217a0001c0001t0004g0014a0001c0001t0004g0040others(10): Show | 15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-127+7251C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525802 | ||||||
chrX:153525855
|
T | TC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7310dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525855 | |||||
chrX:153525884
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(55): Show | 65 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-127+7333G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525884 | ||||||
chrX:153525916
|
GC | G | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-127+7369delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525916 | |||||
chrX:153525963
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(66): Show | 77 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-127+7412T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525963 | ||||||
chrX:153525973
|
T | TG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7425dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153525973 | |||||
chrX:153526075
|
G | A | 31 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(28): Show | 34 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-127+7524G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526075 | ||||||
chrX:153526079
|
T | TA | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7529dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153526079 | |||||
chrX:153526128
|
G | A | 107 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0047others(104): Show | 113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-127+7577G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526128 | ||||||
chrX:153526132
|
G | C | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-127+7581G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526132 | ||||||
chrX:153526145
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7595dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153526145 | |||||
chrX:153526212
|
G | C | 135 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(132): Show | 143 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.-127+7661G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526212 | ||||||
chrX:153526271
|
A | G | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+7720A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526271 | ||||||
chrX:153526430
|
G | A | 1 | a0001c0001t0011g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-127+7879G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526430 | ||||||
chrX:153526430
|
G | GC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7880dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153526430 | |||||
chrX:153526473
|
G | T | 6 | a0001c0001t0007g0237a0001c0001t0009g0236a0001c0001t0049g0083others(3): Show | 6 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+7922G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526473 | ||||||
chrX:153526491
|
T | TG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+7943dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153526491 | |||||
chrX:153526799
|
T | C | 5 | a0001c0001t0022g0233a0001c0001t0051g0017a0001c0003t0047g0100others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+8248T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526799 | ||||||
chrX:153526908
|
G | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+8357G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526908 | ||||||
chrX:153526969
|
G | A | 26 | a0001c0001t0001g0042a0001c0001t0016g0186a0001c0002t0001g0171others(23): Show | 28 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-127+8418G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526969 | ||||||
chrX:153526979
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+8430dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153526979 | |||||
chrX:153527044
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+8494dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527044 | |||||
chrX:153527066
|
G | A | 1 | a0001c0001t0033g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-127+8515G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527066 | ||||||
chrX:153527084
|
A | AT | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+8536dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527084 | |||||
chrX:153527111
|
G | A | 6 | a0001c0001t0007g0237a0001c0001t0009g0236a0001c0001t0049g0083others(3): Show | 6 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+8560G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527111 | ||||||
chrX:153527128
|
A | G | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-127+8577A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527128 | ||||||
chrX:153527177
|
A | AC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-127+8627dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527177 | |||||
chrX:153527368
|
C | CG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-8750dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527368 | |||||
chrX:153527388
|
G | C | 5 | a0001c0001t0001g0244a0001c0001t0046g0243a0001c0002t0001g0242others(2): Show | 5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8734G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527388 | ||||||
chrX:153527453
|
T | A | 20 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(17): Show | 20 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-126-8669T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527453 | ||||||
chrX:153527463
|
G | A | 23 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0217others(20): Show | 25 | HG01361.hp2 HG01884.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-126-8659G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527463 | ||||||
chrX:153527466
|
C | T | 23 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0217others(20): Show | 25 | HG01361.hp2 HG01884.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-126-8656C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527466 | ||||||
chrX:153527522
|
C | T | 134 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(131): Show | 142 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-126-8600C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527522 | ||||||
chrX:153527604
|
A | T | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-8518A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527604 | ||||||
chrX:153527640
|
C | A | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-8482C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527640 | ||||||
chrX:153527691
|
G | A | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126-8431G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527691 | ||||||
chrX:153527700
|
T | TG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-8418dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527700 | |||||
chrX:153527732
|
G | GC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-8385dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527732 | |||||
chrX:153527823
|
T | G | 1 | a0001c0002t0001g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-126-8299T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527823 | ||||||
chrX:153527951
|
T | TG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-8167dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527951 | |||||
chrX:153527981
|
TG | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-8139delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527981 | |||||
chrX:153527985
|
GC | G | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-8134delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153527985 | |||||
chrX:153527997
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0046g0243a0001c0002t0001g0242others(2): Show | 5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8125C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527997 | ||||||
chrX:153528077
|
G | GC | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-8044dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528077 | |||||
chrX:153528100
|
G | T | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-126-8022G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528100 | ||||||
chrX:153528126
|
A | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7996A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528126 | ||||||
chrX:153528163
|
CT | C | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7957delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528163 | |||||
chrX:153528174
|
C | CT | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-7944dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528174 | |||||
chrX:153528206
|
G | GC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-7915dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528206 | |||||
chrX:153528237
|
A | AG | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7884dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528237 | |||||
chrX:153528309
|
T | G | 9 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-7813T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528309 | ||||||
chrX:153528417
|
CT | C | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7703delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528417 | |||||
chrX:153528467
|
AG | A | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-7651delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528467 | |||||
chrX:153528488
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-7632dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528488 | |||||
chrX:153528510
|
G | T | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-7612G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528510 | ||||||
chrX:153528593
|
A | AGACCC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-7528_-126-752 others(9): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528593 | |||||
chrX:153528617
|
G | T | 134 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(131): Show | 142 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-126-7505G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528617 | ||||||
chrX:153528629
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-7493T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528629 | ||||||
chrX:153528721
|
T | A | 2 | a0000c0008t0021g0228a0001c0022t0025g0234 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-7401T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528721 | ||||||
chrX:153528782
|
CACA | C | 2 | a0001c0001t0011g0037a0001c0001t0011g0038 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-126-7339_-126-733 others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528782 | ||||||
chrX:153528803
|
AG | A | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7317delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528803 | |||||
chrX:153528949
|
TA | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7171delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528949 | |||||
chrX:153528981
|
GA | G | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7137delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153528981 | |||||
chrX:153529004
|
G | A | 2 | a0000c0018t0013g0090a0001c0001t0005g0091 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-126-7118G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529004 | ||||||
chrX:153529030
|
GC | G | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7090delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153529030 | |||||
chrX:153529291
|
T | TG | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-6829dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153529291 | |||||
chrX:153529363
|
TC | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-6757delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153529363 | |||||
chrX:153529475
|
G | A | 109 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(106): Show | 115 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-126-6647G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529475 | ||||||
chrX:153529478
|
A | AG | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-6642dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153529478 | |||||
chrX:153529557
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-126-6565G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529557 | ||||||
chrX:153529598
|
T | G | 1 | a0001c0001t0003g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-126-6524T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529598 | ||||||
chrX:153529623
|
G | A | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-6499G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529623 | ||||||
chrX:153529722
|
AG | A | 1 | a0001c0001t0001g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-126-6399delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529722 | ||||||
chrX:153529723
|
G | C | 2 | a0001c0001t0002g0021a0001c0002t0017g0103 | 2 | HG01256.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-126-6399G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529723 | ||||||
chrX:153529744
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-126-6378C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529744 | ||||||
chrX:153529898
|
CT | C | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-6222delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153529898 | |||||
chrX:153530123
|
A | G | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-5999A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530123 | ||||||
chrX:153530124
|
G | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0182 | 2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-126-5998G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530124 | ||||||
chrX:153530279
|
TC | T | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-126-5840delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153530279 | |||||
chrX:153530393
|
G | C | 2 | a0001c0002t0001g0104a0001c0002t0001g0174 | 2 | HG01346.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-126-5729G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530393 | ||||||
chrX:153530629
|
TG | T | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-126-5491delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153530629 | |||||
chrX:153530650
|
G | A | 2 | a0001c0002t0032g0105a0001c0002t0043g0106 | 2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-126-5472G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530650 | ||||||
chrX:153530817
|
G | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00423.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-126-5305G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530817 | ||||||
chrX:153530818
|
G | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0002t0017g0201 | 3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-5304G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530818 | ||||||
chrX:153530938
|
G | A | 5 | a0001c0001t0009g0236a0001c0001t0049g0083a0001c0001t0053g0084others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-5184G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530938 | ||||||
chrX:153530939
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-126-5183A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530939 | ||||||
chrX:153531057
|
A | C | 1 | a0001c0001t0006g0074 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-126-5065A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531057 | ||||||
chrX:153531069
|
G | A | 5 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-5053G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531069 | ||||||
chrX:153531264
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-126-4858C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531264 | ||||||
chrX:153531319
|
TG | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-4800delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153531319 | |||||
chrX:153531442
|
G | A | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-4680G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531442 | ||||||
chrX:153531457
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-126-4665G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531457 | ||||||
chrX:153531512
|
G | A | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126-4610G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531512 | ||||||
chrX:153531636
|
C | T | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-4486C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531636 | ||||||
chrX:153531654
|
T | C | 1 | a0001c0017t0048g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-126-4468T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531654 | ||||||
chrX:153531818
|
G | T | 29 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(26): Show | 32 | HG00642.hp1 HG01934.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.-126-4304G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531818 | ||||||
chrX:153531854
|
A | T | 2 | a0001c0020t0009g0229a0001c0022t0025g0234 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-4268A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531854 | ||||||
chrX:153531858
|
C | G | 239 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0002others(236): Show | 257 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-126-4264C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531858 | ||||||
chrX:153531873
|
G | A | 3 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0002t0017g0201 | 3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-4249G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531873 | ||||||
chrX:153532052
|
AG | A | 2 | a0001c0001t0020g0230a0003c0009t0005g0081 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-126-4068delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153532052 | |||||
chrX:153532217
|
C | T | 1 | a0001c0002t0013g0241 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-126-3905C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532217 | ||||||
chrX:153532241
|
A | AG | 1 | a0001c0001t0033g0214 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-126-3877dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153532241 | |||||
chrX:153532244
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(50): Show | 59 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-126-3878G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532244 | ||||||
chrX:153532408
|
G | A | 1 | a0001c0002t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-126-3714G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532408 | ||||||
chrX:153532414
|
G | A | 5 | a0001c0001t0009g0236a0001c0001t0049g0083a0001c0001t0053g0084others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-3708G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532414 | ||||||
chrX:153532479
|
C | G | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-126-3643C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532479 | ||||||
chrX:153532621
|
G | A | 122 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(119): Show | 130 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-126-3501G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532621 | ||||||
chrX:153532720
|
G | C | 1 | a0001c0021t0019g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-126-3402G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532720 | ||||||
chrX:153532876
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-126-3246C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532876 | ||||||
chrX:153532878
|
G | A | 10 | a0001c0002t0001g0190a0001c0002t0002g0169a0001c0002t0002g0189others(7): Show | 10 | HG00423.hp2 HG02071.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.-126-3244G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532878 | ||||||
chrX:153532890
|
A | G | 2 | a0001c0020t0009g0229a0001c0022t0025g0234 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-3232A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532890 | ||||||
chrX:153532946
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-126-3176G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532946 | ||||||
chrX:153533275
|
C | T | 1 | a0001c0001t0035g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-126-2847C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533275 | ||||||
chrX:153533294
|
G | A | 6 | a0000c0018t0013g0090a0001c0001t0001g0244a0001c0001t0005g0091others(3): Show | 6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-2828G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533294 | ||||||
chrX:153533408
|
G | A | 1 | a0001c0002t0032g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-126-2714G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533408 | ||||||
chrX:153533472
|
A | G | 5 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-2650A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533472 | ||||||
chrX:153533522
|
G | A | 5 | a0001c0001t0009g0236a0001c0001t0049g0083a0001c0001t0053g0084others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-2600G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533522 | ||||||
chrX:153533668
|
A | G | 20 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0161others(17): Show | 20 | HG01361.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-126-2454A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533668 | ||||||
chrX:153533669
|
G | C | 121 | a0000c0013t0041g0041a0001c0001t0001g0042a0001c0001t0001g0047others(118): Show | 129 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-126-2453G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533669 | ||||||
chrX:153533838
|
C | T | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-2284C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533838 | ||||||
chrX:153534167
|
G | A | 1 | a0001c0002t0012g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-126-1955G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534167 | ||||||
chrX:153534194
|
T | TG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-1924dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153534194 | |||||
chrX:153534199
|
AG | A | 13 | a0001c0001t0001g0217a0001c0001t0004g0014a0001c0001t0004g0040others(10): Show | 15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126-1919delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153534199 | |||||
chrX:153534298
|
G | A | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0167others(4): Show | 7 | HG00423.hp1 HG00558.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-1824G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534298 | ||||||
chrX:153534332
|
C | T | 2 | a0000c0018t0013g0090a0001c0001t0005g0091 | 2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-126-1790C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534332 | ||||||
chrX:153534451
|
T | C | 2 | a0001c0001t0022g0233a0001c0011t0023g0232 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-1671T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534451 | ||||||
chrX:153534460
|
CA | C | 98 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0002others(95): Show | 105 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-126-1660delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153534460 | |||||
chrX:153534471
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-126-1651C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534471 | ||||||
chrX:153534526
|
C | T | 2 | a0001c0007t0001g0046a0001c0007t0001g0069 | 2 | NA18944.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-126-1596C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534526 | ||||||
chrX:153534695
|
C | T | 2 | a0001c0002t0001g0159a0001c0002t0001g0160 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-126-1427C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534695 | ||||||
chrX:153534985
|
T | G | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(235): Show | 256 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-126-1137T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534985 | ||||||
chrX:153535050
|
A | G | 9 | a0001c0001t0009g0236a0001c0001t0020g0230a0001c0001t0049g0083others(6): Show | 9 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-1072A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535050 | ||||||
chrX:153535178
|
G | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0002t0017g0201 | 3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-944G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535178 | ||||||
chrX:153535372
|
A | G | 236 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(233): Show | 254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-126-750A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535372 | ||||||
chrX:153535544
|
C | T | 119 | a0000c0013t0041g0041a0001c0001t0001g0042a0001c0001t0001g0047others(116): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-126-578C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535544 | ||||||
chrX:153535562
|
C | T | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-126-560C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535562 | ||||||
chrX:153535602
|
G | A | 2 | a0000c0008t0021g0228a0001c0005t0007g0016 | 3 | HG02976.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-520G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535602 | ||||||
chrX:153535724
|
TG | T | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-126-394delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153535724 | |||||
chrX:153535800
|
TG | T | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-126-316delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153535800 | |||||
chrX:153535842
|
A | G | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(235): Show | 256 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-126-280A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535842 | ||||||
chrX:153535887
|
C | A | 3 | a0001c0001t0001g0161a0001c0001t0035g0070a0003c0009t0005g0081 | 3 | HG02559.hp2 HG03041.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-126-235C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535887 | ||||||
chrX:153536534
|
C | T | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+79C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536534 | ||||||
chrX:153536549
|
T | C | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+94T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536549 | ||||||
chrX:153536583
|
TC | T | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+131delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153536583 | |||||
chrX:153536600
|
G | GC | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+148dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153536600 | |||||
chrX:153536685
|
G | A | 2 | a0001c0002t0002g0188a0001c0002t0002g0199 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.208+230G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536685 | ||||||
chrX:153536897
|
C | G | 1 | a0003c0009t0005g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+442C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536897 | ||||||
chrX:153536963
|
A | AG | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.208+512dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153536963 | |||||
chrX:153536986
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(71): Show | 80 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.208+531G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536986 | ||||||
chrX:153536986
|
G | T | 5 | a0001c0001t0009g0236a0001c0001t0016g0186a0001c0003t0002g0085others(2): Show | 5 | HG00642.hp1 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+531G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536986 | ||||||
chrX:153537122
|
TG | T | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.208+671delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153537122 | |||||
chrX:153537128
|
G | A | 2 | a0001c0002t0001g0009a0004c0019t0001g0114 | 3 | HG00673.hp1 NA19066.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.208+673G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537128 | ||||||
chrX:153537274
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.208+819G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537274 | ||||||
chrX:153537288
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+836dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153537288 | |||||
chrX:153537487
|
G | A | 1 | a0001c0001t0018g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.208+1032G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537487 | ||||||
chrX:153537542
|
A | AG | 2 | a0001c0001t0001g0158a0001c0002t0001g0094 | 2 | NA19060.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.208+1093dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153537542 | |||||
chrX:153537587
|
C | T | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.208+1132C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537587 | ||||||
chrX:153537642
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1187G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537642 | ||||||
chrX:153537678
|
A | C | 1 | a0001c0001t0005g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208+1223A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537678 | ||||||
chrX:153537831
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1376G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537831 | ||||||
chrX:153538096
|
G | A | 4 | a0001c0001t0003g0212a0001c0001t0008g0013a0001c0001t0019g0207others(1): Show | 5 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1641G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538096 | ||||||
chrX:153538136
|
G | A | 11 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.208+1681G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538136 | ||||||
chrX:153538396
|
T | C | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.208+1941T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538396 | ||||||
chrX:153538414
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1959G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538414 | ||||||
chrX:153538502
|
C | T | 2 | a0001c0001t0020g0230a0003c0009t0005g0081 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208+2047C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538502 | ||||||
chrX:153538520
|
TC | T | 1 | a0001c0001t0004g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.208+2066delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538520 | ||||||
chrX:153538593
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+2138C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538593 | ||||||
chrX:153538786
|
C | G | 1 | a0001c0001t0005g0035 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+2331C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538786 | ||||||
chrX:153538814
|
G | A | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+2359G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538814 | ||||||
chrX:153538908
|
G | A | 30 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0001g0204others(27): Show | 34 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.209-2451G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538908 | ||||||
chrX:153538960
|
C | G | 1 | a0001c0002t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.209-2399C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538960 | ||||||
chrX:153539139
|
T | TC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.209-2216dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153539139 | |||||
chrX:153539191
|
G | A | 1 | a0001c0002t0001g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.209-2168G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539191 | ||||||
chrX:153539293
|
C | T | 6 | a0000c0018t0013g0090a0001c0001t0001g0244a0001c0001t0005g0091others(3): Show | 6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2066C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539293 | ||||||
chrX:153539360
|
T | C | 1 | a0001c0002t0002g0193 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.209-1999T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539360 | ||||||
chrX:153539594
|
C | G | 1 | a0001c0002t0045g0157 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.209-1765C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539594 | ||||||
chrX:153539624
|
C | T | 141 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0042others(138): Show | 149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.209-1735C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539624 | ||||||
chrX:153539684
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(71): Show | 80 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.209-1675T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539684 | ||||||
chrX:153539737
|
C | T | 19 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0113others(16): Show | 19 | HG01361.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.209-1622C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539737 | ||||||
chrX:153539795
|
T | TC | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.209-1561dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153539795 | |||||
chrX:153539812
|
G | A | 1 | a0001c0003t0026g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.209-1547G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539812 | ||||||
chrX:153539823
|
G | A | 26 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(23): Show | 30 | HG00735.hp2 HG01934.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1536G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539823 | ||||||
chrX:153539902
|
A | G | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.209-1457A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539902 | ||||||
chrX:153540004
|
A | C | 1 | a0001c0001t0002g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.209-1355A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540004 | ||||||
chrX:153540286
|
A | T | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-1073A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540286 | ||||||
chrX:153540431
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0204 | 2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.209-928C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540431 | ||||||
chrX:153540498
|
TC | T | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.209-857delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540498 | |||||
chrX:153540539
|
G | T | 1 | a0001c0002t0002g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209-820G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540539 | ||||||
chrX:153540687
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-672G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540687 | ||||||
chrX:153540713
|
AG | A | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.209-640delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540713 | |||||
chrX:153540790
|
GC | G | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.209-566delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540790 | |||||
chrX:153540886
|
CCT | C | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.209-471_209-470del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540886 | |||||
chrX:153540994
|
TCC | T | 4 | a0001c0001t0015g0227a0001c0004t0007g0226a0001c0004t0009g0239others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-362_209-361del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540994 | |||||
chrX:153541111
|
G | A | 1 | a0001c0002t0002g0180 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.209-248G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541111 | ||||||
chrX:153541155
|
G | A | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209-204G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541155 | ||||||
chrX:153541170
|
C | T | 21 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(18): Show | 24 | HG00735.hp2 HG01934.hp1 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.209-189C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541170 | ||||||
chrX:153541236
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-123G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541236 | ||||||
chrX:153541328
|
TC | T | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.209-27delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153541328 | |||||
chrX:153541576
|
G | A | 13 | a0001c0001t0001g0161a0001c0001t0001g0206a0001c0001t0001g0208others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+20G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/21 | chrX | 153541576 | ||||||
chrX:153541663
|
G | A | 2 | a0000c0008t0021g0228a0003c0009t0005g0081 | 2 | HG02976.hp2 HG03041.hp2 |
splice_region_variant&intron_variant | LOW | c.407-6G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/21 | chrX | 153541663 | ||||||
chrX:153541967
|
G | A | 125 | a0000c0013t0041g0041a0001c0001t0001g0042a0001c0001t0001g0047others(122): Show | 133 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.664+41G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153541967 | ||||||
chrX:153542046
|
CCTT | C | 169 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(166): Show | 181 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.664+121_664+123del others(3): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542046 | ||||||
chrX:153542049
|
TAGGAGGC others(64): Show |
T | 79 | a0000c0008t0021g0228a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 85 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.664+124_664+194del others(71): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542049 | ||||||
chrX:153542060
|
A | AG | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+136dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542060 | |||||
chrX:153542071
|
G | GGT | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+145_664+146ins others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542071 | ||||||
chrX:153542072
|
T | G | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+146T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542072 | ||||||
chrX:153542081
|
T | TA | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+155_664+156ins others(1): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542081 | ||||||
chrX:153542099
|
G | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.664+173G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542099 | ||||||
chrX:153542106
|
TG | T | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+182delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542106 | |||||
chrX:153542168
|
TC | T | 160 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0042others(157): Show | 172 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.665-149delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542168 | |||||
chrX:153542168
|
TCC | T | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.665-150_665-149del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542168 | |||||
chrX:153542207
|
A | G | 237 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0002others(234): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.665-116A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542207 | ||||||
chrX:153542262
|
T | C | 8 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542262 | ||||||
chrX:153542289
|
TG | T | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.665-30delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542289 | |||||
chrX:153542465
|
G | C | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.790+17G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542465 | ||||||
chrX:153542488
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0162a0001c0022t0025g0234 | 3 | HG02896.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.790+40G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542488 | ||||||
chrX:153542662
|
G | A | 240 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(237): Show | 258 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.790+214G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542662 | ||||||
chrX:153542683
|
A | G | 1 | a0001c0003t0024g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790+235A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542683 | ||||||
chrX:153542761
|
T | A | 23 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(20): Show | 27 | HG00735.hp2 HG01934.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.791-282T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542761 | ||||||
chrX:153542884
|
G | A | 2 | a0001c0001t0011g0036a0001c0011t0023g0232 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.791-159G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542884 | ||||||
chrX:153542951
|
CG | C | 1 | a0007c0023t0001g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.791-89delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chrX | 153542951 | |||||
chrX:153543244
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916+76G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543244 | ||||||
chrX:153543421
|
C | T | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.916+253C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543421 | ||||||
chrX:153543490
|
C | T | 23 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(20): Show | 27 | HG00735.hp2 HG01934.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.916+322C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543490 | ||||||
chrX:153543607
|
A | C | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.916+439A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543607 | ||||||
chrX:153543677
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.916+509G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543677 | ||||||
chrX:153543745
|
T | G | 25 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(22): Show | 29 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.916+577T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543745 | ||||||
chrX:153543776
|
T | C | 243 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(240): Show | 261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.916+608T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543776 | ||||||
chrX:153543852
|
C | T | 1 | a0001c0001t0007g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.916+684C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543852 | ||||||
chrX:153544169
|
G | T | 1 | a0001c0002t0001g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.916+1001G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544169 | ||||||
chrX:153544284
|
T | C | 8 | a0000c0018t0013g0090a0001c0001t0001g0202a0001c0001t0001g0204others(5): Show | 8 | HG00609.hp1 HG00741.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.916+1116T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544284 | ||||||
chrX:153544378
|
C | T | 2 | a0001c0001t0027g0240a0001c0010t0005g0173 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.916+1210C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544378 | ||||||
chrX:153544564
|
G | A | 6 | a0000c0018t0013g0090a0001c0001t0001g0244a0001c0001t0005g0091others(3): Show | 6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.916+1396G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544564 | ||||||
chrX:153544787
|
C | G | 1 | a0001c0001t0004g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.917-1301C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544787 | ||||||
chrX:153544814
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.917-1274G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544814 | ||||||
chrX:153544850
|
C | T | 19 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(16): Show | 22 | HG00642.hp1 HG01934.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.917-1238C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544850 | ||||||
chrX:153544994
|
G | A | 27 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0082others(24): Show | 30 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.917-1094G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544994 | ||||||
chrX:153545066
|
A | G | 1 | a0001c0015t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.917-1022A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545066 | ||||||
chrX:153545092
|
C | CG | 4 | a0001c0001t0001g0067a0001c0001t0001g0206a0001c0002t0040g0068others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.917-986dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545092 | |||||
chrX:153545092
|
CG | C | 168 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0005others(165): Show | 182 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.917-986delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545092 | |||||
chrX:153545092
|
CGG | C | 1 | a0001c0001t0005g0035 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.917-987_917-986del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545092 | |||||
chrX:153545096
|
G | T | 1 | a0001c0001t0013g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.917-992G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545096 | ||||||
chrX:153545127
|
G | A | 1 | a0001c0002t0002g0200 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.917-961G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545127 | ||||||
chrX:153545347
|
T | A | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.917-741T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545347 | ||||||
chrX:153545363
|
C | T | 1 | a0001c0021t0019g0075 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917-725C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545363 | ||||||
chrX:153545499
|
C | T | 5 | a0001c0001t0011g0037a0001c0001t0011g0038a0001c0001t0049g0083others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.917-589C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545499 | ||||||
chrX:153545500
|
G | A | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.917-588G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545500 | ||||||
chrX:153545516
|
CA | C | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.917-567delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545516 | |||||
chrX:153545599
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.917-489A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545599 | ||||||
chrX:153545628
|
C | T | 21 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(18): Show | 24 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.917-460C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545628 | ||||||
chrX:153545747
|
G | A | 17 | a0000c0018t0013g0090a0001c0001t0001g0161a0001c0001t0001g0206others(14): Show | 17 | HG00609.hp1 HG00741.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.917-341G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545747 | ||||||
chrX:153545765
|
G | A | 2 | a0001c0001t0019g0207a0001c0005t0007g0016 | 3 | HG02818.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.917-323G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545765 | ||||||
chrX:153545773
|
T | C | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.917-315T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545773 | ||||||
chrX:153545953
|
C | CG | 1 | a0001c0002t0001g0098 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.917-131dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545953 | |||||
chrX:153546029
|
C | T | 2 | a0001c0003t0001g0033a0001c0022t0025g0234 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.917-59C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153546029 | ||||||
chrX:153546226
|
G | T | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.958+97G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546226 | ||||||
chrX:153546414
|
C | T | 1 | a0001c0002t0001g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.958+285C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546414 | ||||||
chrX:153546430
|
T | C | 29 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0002t0001g0109others(26): Show | 31 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.958+301T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546430 | ||||||
chrX:153546716
|
C | G | 22 | a0001c0001t0001g0082a0001c0001t0001g0210a0001c0001t0001g0217others(19): Show | 25 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.958+587C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546716 | ||||||
chrX:153546814
|
G | A | 2 | a0001c0001t0011g0036a0001c0011t0023g0232 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.958+685G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546814 | ||||||
chrX:153546929
|
G | T | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.958+800G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546929 | ||||||
chrX:153547333
|
G | A | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959-502G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153547333 | ||||||
chrX:153547496
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959-339C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153547496 | ||||||
chrX:153547701
|
T | TTG | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.959-133_959-132dup others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chrX | 153547701 | |||||
chrX:153548017
|
T | G | 5 | a0001c0001t0001g0078a0001c0003t0001g0033a0001c0003t0001g0034others(2): Show | 5 | HG01361.hp2 HG02647.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123+18T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548017 | ||||||
chrX:153548057
|
G | C | 8 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123+58G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548057 | ||||||
chrX:153548165
|
G | A | 2 | a0000c0008t0021g0228a0001c0011t0023g0232 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1123+166G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548165 | ||||||
chrX:153548281
|
CT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(61): Show | 68 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1123+283delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548281 | ||||||
chrX:153548288
|
C | A | 19 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0002g0184others(16): Show | 19 | HG00741.hp1 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1123+289C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548288 | ||||||
chrX:153548302
|
TG | T | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1123+308delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 153548302 | |||||
chrX:153548322
|
A | AC | 3 | a0001c0001t0014g0064a0001c0002t0001g0150a0001c0002t0003g0149 | 3 | HG00621.hp1 HG00735.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1124-314dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 153548322 | |||||
chrX:153548367
|
TC | T | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1124-269delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chrX | 153548367 | |||||
chrX:153548915
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(93): Show | 107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1338+61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153548915 | ||||||
chrX:153549012
|
TCTGTCAG others(4): Show |
T | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1338+159_1338+169d others(13): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549012 | ||||||
chrX:153549198
|
TGTGGGGT others(1): Show |
T | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1339-273_1339-266d others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 153549198 | |||||
chrX:153549224
|
T | TG | 1 | a0001c0002t0014g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1339-269dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 153549224 | |||||
chrX:153549282
|
TC | T | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1339-212delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chrX | 153549282 | |||||
chrX:153549299
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1339-198G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549299 | ||||||
chrX:153549305
|
A | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0082others(20): Show | 23 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1339-192A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549305 | ||||||
chrX:153549418
|
C | T | 3 | a0000c0008t0021g0228a0001c0001t0022g0233a0001c0011t0023g0232 | 3 | HG02809.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1339-79C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549418 | ||||||
chrX:153549837
|
G | GC | 1 | a0001c0001t0002g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1581+105dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chrX | 153549837 | |||||
chrX:153549964
|
G | C | 5 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1582-81G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 11/21 | chrX | 153549964 | ||||||
chrX:153550343
|
G | A | 9 | a0000c0018t0013g0090a0001c0001t0001g0125a0001c0001t0001g0210others(6): Show | 9 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1823+57G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550343 | ||||||
chrX:153550417
|
G | A | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1823+131G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550417 | ||||||
chrX:153550426
|
A | G | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1823+140A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550426 | ||||||
chrX:153550428
|
C | T | 111 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(108): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1823+142C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550428 | ||||||
chrX:153550512
|
G | GC | 1 | a0001c0001t0002g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1823+230dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153550512 | |||||
chrX:153550553
|
GC | G | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+269delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153550553 | |||||
chrX:153550581
|
C | G | 11 | a0000c0018t0013g0090a0001c0001t0001g0078a0001c0001t0001g0079others(8): Show | 11 | HG00741.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1823+295C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550581 | ||||||
chrX:153550645
|
T | C | 193 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(190): Show | 204 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1823+359T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550645 | ||||||
chrX:153550669
|
T | TTTTTG | 4 | a0001c0001t0001g0217a0001c0001t0004g0040a0001c0001t0033g0214others(1): Show | 4 | NA18939.hp1 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+398_1823+402d others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153550669 | |||||
chrX:153550748
|
C | T | 69 | a0000c0008t0021g0228a0001c0001t0001g0003a0001c0001t0001g0027others(66): Show | 71 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1823+462C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550748 | ||||||
chrX:153550761
|
G | A | 111 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(108): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1823+475G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550761 | ||||||
chrX:153550835
|
G | A | 4 | a0001c0001t0002g0039a0001c0001t0002g0055a0001c0001t0010g0007others(1): Show | 4 | HG00544.hp2 NA18979.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+549G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550835 | ||||||
chrX:153550989
|
G | A | 111 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(108): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1823+703G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550989 | ||||||
chrX:153551006
|
TC | T | 8 | a0000c0008t0021g0228a0001c0001t0001g0042a0001c0001t0001g0202others(5): Show | 8 | HG02257.hp2 HG02735.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1823+721delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551006 | ||||||
chrX:153551008
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0216 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1823+722G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551008 | ||||||
chrX:153551012
|
C | CCA | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+728_1823+729d others(4): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551012 | |||||
chrX:153551033
|
T | TC | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+748dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551033 | |||||
chrX:153551125
|
C | T | 111 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(108): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1823+839C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551125 | ||||||
chrX:153551128
|
G | A | 111 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(108): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1823+842G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551128 | ||||||
chrX:153551143
|
G | C | 2 | a0001c0003t0007g0231a0001c0003t0034g0029 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1823+857G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551143 | ||||||
chrX:153551164
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1823+878G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551164 | ||||||
chrX:153551212
|
C | G | 11 | a0000c0018t0013g0090a0001c0001t0001g0125a0001c0001t0001g0210others(8): Show | 11 | HG00741.hp1 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1823+926C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551212 | ||||||
chrX:153551226
|
AT | A | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+944delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551226 | |||||
chrX:153551388
|
GC | G | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823+1105delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551388 | |||||
chrX:153551395
|
G | T | 1 | a0001c0002t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1823+1109G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551395 | ||||||
chrX:153551506
|
A | G | 2 | a0001c0002t0012g0088a0001c0002t0012g0089 | 2 | NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1823+1220A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551506 | ||||||
chrX:153551573
|
C | T | 11 | a0001c0001t0001g0217a0001c0001t0004g0014a0001c0001t0004g0040others(8): Show | 12 | NA18612.hp1 NA18939.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1823+1287C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551573 | ||||||
chrX:153551574
|
G | A | 2 | a0001c0003t0002g0085a0003c0009t0005g0081 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1823+1288G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551574 | ||||||
chrX:153551601
|
GCTTAGAG others(14): Show |
G | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1823+1339_1823+135 others(25): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551601 | |||||
chrX:153551699
|
C | T | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(235): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1824-1336C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551699 | ||||||
chrX:153551732
|
G | T | 4 | a0001c0002t0002g0169a0001c0002t0014g0099a0001c0002t0029g0019others(1): Show | 4 | NA18950.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-1303G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551732 | ||||||
chrX:153551761
|
TAGAACAA | T | 1 | a0001c0001t0027g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1824-1271_1824-126 others(11): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551761 | |||||
chrX:153551804
|
C | T | 2 | a0001c0002t0001g0077a0001c0002t0016g0076 | 2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1824-1231C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551804 | ||||||
chrX:153551832
|
C | G | 1 | a0001c0001t0004g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1824-1203C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551832 | ||||||
chrX:153551892
|
C | G | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1143C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551892 | ||||||
chrX:153551893
|
T | G | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1142T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551893 | ||||||
chrX:153551894
|
G | T | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1141G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551894 | ||||||
chrX:153551895
|
C | G | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1140C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551895 | ||||||
chrX:153551897
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1824-1138G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551897 | ||||||
chrX:153551932
|
C | G | 1 | a0001c0001t0027g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1824-1103C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551932 | ||||||
chrX:153552014
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1824-1021G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552014 | ||||||
chrX:153552032
|
T | TC | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1824-1000dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552032 | |||||
chrX:153552113
|
G | A | 243 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(240): Show | 260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1824-922G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552113 | ||||||
chrX:153552114
|
C | A | 243 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(240): Show | 260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1824-921C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552114 | ||||||
chrX:153552172
|
C | T | 1 | a0001c0002t0002g0170 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1824-863C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552172 | ||||||
chrX:153552205
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1824-830T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552205 | ||||||
chrX:153552274
|
AG | A | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1824-758delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552274 | |||||
chrX:153552281
|
C | T | 4 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0002g0031others(1): Show | 4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-754C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552281 | ||||||
chrX:153552309
|
T | C | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1824-726T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552309 | ||||||
chrX:153552333
|
T | G | 4 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0002g0031others(1): Show | 4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-702T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552333 | ||||||
chrX:153552480
|
CT | C | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1824-551delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552480 | |||||
chrX:153552492
|
T | TC | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1824-541dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552492 | |||||
chrX:153552536
|
G | A | 1 | a0001c0001t0046g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1824-499G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552536 | ||||||
chrX:153552577
|
G | GT | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1824-456dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552577 | |||||
chrX:153552581
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1824-454C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552581 | ||||||
chrX:153552662
|
G | A | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1824-373G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552662 | ||||||
chrX:153552679
|
T | C | 4 | a0001c0003t0001g0033a0001c0003t0001g0034a0001c0003t0002g0031others(1): Show | 4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-356T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552679 | ||||||
chrX:153552721
|
G | C | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1824-314G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552721 | ||||||
chrX:153552857
|
C | A | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1824-178C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552857 | ||||||
chrX:153552889
|
TC | T | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1824-143delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552889 | |||||
chrX:153552966
|
G | GT | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1824-68dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153552966 | |||||
chrX:153552977
|
G | A | 110 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(107): Show | 119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1824-58G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552977 | ||||||
chrX:153553369
|
C | CG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+102dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153553369 | |||||
chrX:153553432
|
G | T | 181 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0003others(178): Show | 192 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.2058+163G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553432 | ||||||
chrX:153553523
|
G | A | 7 | a0000c0018t0013g0090a0001c0001t0001g0125a0001c0001t0002g0184others(4): Show | 7 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+254G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553523 | ||||||
chrX:153553592
|
A | AG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+327dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153553592 | |||||
chrX:153553616
|
G | GGT | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+349_2058+350d others(4): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153553616 | |||||
chrX:153553655
|
C | G | 114 | a0000c0013t0041g0041a0001c0001t0001g0127a0001c0001t0001g0158others(111): Show | 123 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.2058+386C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553655 | ||||||
chrX:153553658
|
C | T | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(235): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.2058+389C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553658 | ||||||
chrX:153553778
|
G | A | 2 | a0001c0002t0001g0065a0001c0002t0003g0126 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2058+509G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553778 | ||||||
chrX:153553779
|
C | T | 1 | a0001c0001t0005g0035 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2058+510C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553779 | ||||||
chrX:153553780
|
G | A | 2 | a0001c0003t0002g0085a0003c0009t0005g0081 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2058+511G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553780 | ||||||
chrX:153553792
|
A | G | 1 | a0001c0002t0002g0147 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2058+523A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553792 | ||||||
chrX:153553816
|
T | G | 1 | a0001c0001t0046g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2058+547T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553816 | ||||||
chrX:153553891
|
G | A | 2 | a0001c0001t0005g0092a0001c0001t0005g0162 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2058+622G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553891 | ||||||
chrX:153553988
|
T | TG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+724dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153553988 | |||||
chrX:153554103
|
C | T | 1 | a0001c0001t0019g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2058+834C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554103 | ||||||
chrX:153554136
|
C | T | 2 | a0001c0003t0002g0085a0003c0009t0005g0081 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2058+867C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554136 | ||||||
chrX:153554208
|
T | TG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+941dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153554208 | |||||
chrX:153554214
|
C | A | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2058+945C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554214 | ||||||
chrX:153554487
|
G | T | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(235): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.2058+1218G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554487 | ||||||
chrX:153554517
|
G | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 14 | HG01109.hp1 HG02258.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2058+1248G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554517 | ||||||
chrX:153554519
|
A | AG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+1252dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153554519 | |||||
chrX:153554553
|
T | TG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2058+1286dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153554553 | |||||
chrX:153554751
|
T | TG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2059-1295dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153554751 | |||||
chrX:153554847
|
C | T | 108 | a0000c0013t0041g0041a0001c0001t0005g0130a0001c0001t0019g0207others(105): Show | 117 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.2059-1202C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554847 | ||||||
chrX:153554904
|
CA | C | 12 | a0001c0001t0020g0230a0001c0001t0022g0233a0001c0003t0001g0033others(9): Show | 13 | HG01243.hp1 HG01361.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2059-1144delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554904 | ||||||
chrX:153554939
|
G | A | 1 | a0001c0001t0027g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2059-1110G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554939 | ||||||
chrX:153555007
|
A | AGG | 1 | a0001c0001t0042g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2059-1040_2059-103 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153555007 | |||||
chrX:153555030
|
AAGG | A | 1 | a0001c0001t0019g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2059-1016_2059-101 others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153555030 | |||||
chrX:153555118
|
T | G | 11 | a0000c0018t0013g0090a0001c0001t0001g0125a0001c0001t0001g0210others(8): Show | 11 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2059-931T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555118 | ||||||
chrX:153555705
|
G | A | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.2059-344G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555705 | ||||||
chrX:153555792
|
A | ATGCAACA others(4): Show |
2 | a0001c0003t0002g0085a0003c0009t0005g0081 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2059-254_2059-253i others(13): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153555792 | |||||
chrX:153555807
|
A | G | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2059-242A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555807 | ||||||
chrX:153555953
|
TG | T | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2059-93delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153555953 | |||||
chrX:153555988
|
T | C | 1 | a0001c0002t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2059-61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555988 | ||||||
chrX:153556005
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0003g0096 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2059-44C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153556005 | ||||||
chrX:153556255
|
G | C | 1 | a0001c0002t0010g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2238+27G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/21 | chrX | 153556255 | ||||||
chrX:153556259
|
C | A | 9 | a0000c0018t0013g0090a0001c0001t0001g0125a0001c0001t0001g0210others(6): Show | 9 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2238+31C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/21 | chrX | 153556259 | ||||||
chrX:153556429
|
C | T | 238 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(235): Show | 255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.2326+11C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556429 | ||||||
chrX:153556438
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 54 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.2326+20C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556438 | ||||||
chrX:153556445
|
T | TG | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2326+31dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | 153556445 | |||||
chrX:153556604
|
G | A | 1 | a0001c0001t0006g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2326+186G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556604 | ||||||
chrX:153556696
|
A | G | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2327-221A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556696 | ||||||
chrX:153556732
|
GCTTA | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2327-180_2327-177d others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chrX | 153556732 | |||||
chrX:153557272
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2433+249G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557272 | ||||||
chrX:153557318
|
C | T | 1 | a0001c0001t0046g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2433+295C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557318 | ||||||
chrX:153557724
|
T | TC | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2434-384dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557724 | |||||
chrX:153557859
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(40): Show | 49 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.2434-253C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557859 | ||||||
chrX:153557881
|
A | AGC | 8 | a0001c0002t0001g0131a0001c0002t0002g0193a0001c0002t0002g0194others(5): Show | 8 | HG00639.hp2 HG00741.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2434-230_2434-229d others(4): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557881 | |||||
chrX:153557882
|
G | GC | 10 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0027others(7): Show | 10 | HG00597.hp1 HG02257.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2434-219dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | |||||
chrX:153557882
|
G | GCGC | 78 | a0000c0013t0041g0041a0001c0001t0019g0207a0001c0002t0001g0001others(75): Show | 87 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | |||||
chrX:153557882
|
G | GCGCC | 26 | a0001c0002t0001g0066a0001c0002t0001g0086a0001c0002t0001g0110others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | |||||
chrX:153557882
|
GC | G | 1 | a0001c0001t0001g0045 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2434-219delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | |||||
chrX:153557883
|
C | CG | 5 | a0001c0001t0051g0017a0001c0003t0026g0235a0001c0003t0047g0100others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(3): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557883 | ||||||
chrX:153557905
|
T | C | 8 | a0001c0001t0051g0017a0001c0003t0002g0085a0001c0003t0002g0211others(5): Show | 8 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2434-207T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557905 | ||||||
chrX:153557941
|
AT | A | 8 | a0001c0001t0051g0017a0001c0003t0002g0085a0001c0003t0002g0211others(5): Show | 8 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2434-169delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557941 | |||||
chrX:153558050
|
A | AG | 1 | a0001c0016t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2434-56dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153558050 | |||||
chrX:153558445
|
T | C | 1 | a0000c0013t0041g0041 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2625+142T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558445 | ||||||
chrX:153558718
|
T | C | 4 | a0001c0002t0002g0169a0001c0002t0014g0099a0001c0002t0029g0019others(1): Show | 4 | NA18950.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2625+415T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558718 | ||||||
chrX:153558744
|
A | T | 15 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(12): Show | 15 | HG00741.hp1 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2625+441A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558744 | ||||||
chrX:153558816
|
C | T | 128 | a0000c0013t0041g0041a0000c0018t0013g0090a0001c0001t0001g0125others(125): Show | 137 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.2625+513C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558816 | ||||||
chrX:153558836
|
G | C | 3 | a0000c0018t0013g0090a0001c0001t0005g0091a0001c0001t0005g0130 | 3 | HG03834.hp2 HG03927.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2625+533G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558836 | ||||||
chrX:153558884
|
T | C | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2625+581T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558884 | ||||||
chrX:153558929
|
A | C | 8 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(5): Show | 8 | HG00741.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2625+626A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558929 | ||||||
chrX:153558972
|
A | G | 61 | a0000c0008t0021g0228a0001c0001t0001g0002a0001c0001t0001g0005others(58): Show | 68 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(65): Show |
intron_variant | MODIFIER | c.2625+669A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558972 | ||||||
chrX:153559049
|
TA | T | 244 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(241): Show | 262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.2626-674delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 153559049 | |||||
chrX:153559334
|
G | C | 193 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(190): Show | 209 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.2626-395G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559334 | ||||||
chrX:153559558
|
G | C | 3 | a0001c0001t0002g0164a0001c0001t0005g0162a0001c0001t0005g0163 | 3 | HG03098.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2626-171G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559558 | ||||||
chrX:153559652
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0005g0209 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2626-77C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559652 | ||||||
chrX:153559707
|
GGT | G | 1 | a0001c0005t0007g0016 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2626-20_2626-19del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 153559707 | |||||
chrX:153559956
|
G | T | 217 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.2839+14G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153559956 | ||||||
chrX:153559975
|
A | G | 243 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(240): Show | 261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.2839+33A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153559975 | ||||||
chrX:153560047
|
C | T | 2 | a0001c0001t0001g0123a0005c0012t0044g0224 | 2 | HG01167.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2839+105C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560047 | ||||||
chrX:153560175
|
G | C | 221 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 239 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2839+233G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560175 | ||||||
chrX:153560364
|
T | TG | 2 | a0001c0002t0001g0098a0001c0016t0002g0198 | 2 | HG01192.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2840-306dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 153560364 | |||||
chrX:153560364
|
TG | T | 7 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(4): Show | 7 | HG00741.hp1 HG02451.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2840-306delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 153560364 | |||||
chrX:153560415
|
C | T | 8 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(5): Show | 8 | HG00741.hp1 HG02071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2840-261C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560415 | ||||||
chrX:153560542
|
T | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 118 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2840-134T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560542 | ||||||
chrX:153560547
|
C | G | 1 | a0001c0001t0008g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2840-129C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560547 | ||||||
chrX:153560548
|
G | A | 3 | a0001c0003t0026g0235a0001c0003t0047g0100a0001c0010t0005g0173 | 3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2840-128G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560548 | ||||||
chrX:153560627
|
C | T | 1 | a0001c0003t0024g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2840-49C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560627 | ||||||
chrX:153561081
|
T | G | 2 | a0001c0002t0017g0103a0001c0002t0017g0201 | 2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.3051+194T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561081 | ||||||
chrX:153561105
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3051+218C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561105 | ||||||
chrX:153561134
|
C | T | 9 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(6): Show | 9 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3051+247C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561134 | ||||||
chrX:153561369
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3051+482A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561369 | ||||||
chrX:153561573
|
A | G | 233 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(230): Show | 251 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3052-562A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561573 | ||||||
chrX:153561584
|
G | T | 233 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(230): Show | 251 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3052-551G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561584 | ||||||
chrX:153561632
|
G | T | 1 | a0003c0009t0005g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3052-503G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561632 | ||||||
chrX:153561847
|
G | A | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3052-288G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561847 | ||||||
chrX:153561987
|
A | G | 233 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(230): Show | 251 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3052-148A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561987 | ||||||
chrX:153561989
|
G | GC | 2 | a0001c0001t0031g0057a0001c0016t0002g0198 | 2 | HG02135.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3052-141dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chrX | 153561989 | |||||
chrX:153561995
|
G | A | 3 | a0001c0003t0026g0235a0001c0003t0047g0100a0001c0010t0005g0173 | 3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3052-140G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561995 | ||||||
chrX:153562130
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0121others(2): Show | 5 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.3052-5C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153562130 | ||||||
chrX:153562452
|
A | G | 3 | a0001c0001t0016g0186a0001c0002t0001g0077a0001c0002t0016g0076 | 3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3159+210A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562452 | ||||||
chrX:153562472
|
G | A | 3 | a0001c0003t0002g0085a0001c0003t0002g0211a0003c0009t0005g0081 | 3 | HG01934.hp1 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3159+230G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562472 | ||||||
chrX:153562508
|
C | T | 1 | a0001c0003t0047g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3159+266C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562508 | ||||||
chrX:153562660
|
G | A | 1 | a0001c0002t0001g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3159+418G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562660 | ||||||
chrX:153562703
|
T | C | 110 | a0000c0013t0041g0041a0001c0001t0001g0078a0001c0001t0001g0079others(107): Show | 118 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.3159+461T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562703 | ||||||
chrX:153562728
|
G | C | 3 | a0001c0001t0016g0186a0001c0002t0001g0077a0001c0002t0016g0076 | 3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3159+486G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562728 | ||||||
chrX:153562819
|
A | T | 1 | a0001c0002t0001g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3159+577A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562819 | ||||||
chrX:153563127
|
T | C | 225 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(222): Show | 241 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.3159+885T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563127 | ||||||
chrX:153563136
|
C | CTTT | 25 | a0000c0008t0021g0228a0001c0001t0001g0005a0001c0001t0001g0059others(22): Show | 27 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.3159+915_3159+917d others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563136
|
C | CTTTT | 190 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 205 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.3159+914_3159+917d others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563136
|
C | CTTTTT | 14 | a0001c0001t0001g0026a0001c0001t0001g0125a0001c0001t0001g0167others(11): Show | 14 | HG00423.hp1 HG01123.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3159+913_3159+917d others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563136
|
C | CTTTTTT | 2 | a0001c0002t0002g0187a0001c0010t0005g0173 | 2 | HG02055.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.3159+912_3159+917d others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563136
|
CT | C | 15 | a0000c0018t0013g0090a0001c0001t0001g0027a0001c0001t0001g0030others(12): Show | 16 | HG00741.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3159+917delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563136
|
CTTTT | C | 1 | a0001c0003t0052g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3159+914_3159+917d others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | |||||
chrX:153563243
|
G | T | 1 | a0001c0002t0003g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3159+1001G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563243 | ||||||
chrX:153563421
|
G | T | 9 | a0000c0008t0021g0228a0001c0003t0001g0033a0001c0003t0001g0034others(6): Show | 9 | HG01361.hp2 HG02257.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3159+1179G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563421 | ||||||
chrX:153563606
|
G | A | 10 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(7): Show | 11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3160-1315G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563606 | ||||||
chrX:153563811
|
T | G | 3 | a0001c0002t0001g0098a0001c0002t0001g0134a0001c0002t0001g0171 | 3 | HG01192.hp1 HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.3160-1110T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563811 | ||||||
chrX:153563940
|
C | T | 103 | a0000c0013t0041g0041a0001c0001t0001g0078a0001c0001t0001g0079others(100): Show | 111 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.3160-981C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563940 | ||||||
chrX:153564118
|
C | T | 10 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(7): Show | 11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3160-803C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564118 | ||||||
chrX:153564167
|
TC | T | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3160-752delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153564167 | |||||
chrX:153564252
|
T | TC | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3160-666dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153564252 | |||||
chrX:153564316
|
C | T | 106 | a0000c0013t0041g0041a0001c0001t0001g0078a0001c0001t0001g0079others(103): Show | 114 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.3160-605C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564316 | ||||||
chrX:153564328
|
C | CT | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3160-589dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153564328 | |||||
chrX:153564464
|
C | G | 1 | a0001c0003t0024g0238 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3160-457C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564464 | ||||||
chrX:153564543
|
G | A | 1 | a0001c0001t0027g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3160-378G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564543 | ||||||
chrX:153564715
|
GC | G | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3160-200delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153564715 | |||||
chrX:153564722
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0022g0233 | 3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3160-199G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564722 | ||||||
chrX:153564864
|
A | G | 233 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(230): Show | 250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3160-57A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564864 | ||||||
chrX:153565197
|
G | A | 4 | a0000c0008t0021g0228a0001c0003t0026g0235a0001c0003t0047g0100others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+94G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565197 | ||||||
chrX:153565226
|
C | T | 228 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(225): Show | 245 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.3342+123C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565226 | ||||||
chrX:153565304
|
A | G | 247 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(244): Show | 265 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.3342+201A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565304 | ||||||
chrX:153565306
|
C | T | 3 | a0001c0001t0020g0230a0001c0004t0007g0226a0001c0004t0015g0225 | 3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+203C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565306 | ||||||
chrX:153565307
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0039g0056 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3342+204G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565307 | ||||||
chrX:153565434
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3342+331T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565434 | ||||||
chrX:153565525
|
T | A | 231 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(228): Show | 248 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.3342+422T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565525 | ||||||
chrX:153565543
|
T | TG | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+444dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153565543 | |||||
chrX:153565590
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(107): Show | 119 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.3342+487T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565590 | ||||||
chrX:153565609
|
C | G | 13 | a0000c0008t0021g0228a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 13 | HG01361.hp2 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3342+506C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565609 | ||||||
chrX:153565687
|
T | C | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3342+584T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565687 | ||||||
chrX:153565740
|
C | T | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3342+637C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565740 | ||||||
chrX:153565791
|
TG | T | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+690delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153565791 | |||||
chrX:153566041
|
A | AG | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3342+941dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566041 | |||||
chrX:153566257
|
GC | G | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+1158delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566257 | |||||
chrX:153566307
|
A | G | 219 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 236 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.3342+1204A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566307 | ||||||
chrX:153566338
|
AG | A | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+1238delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566338 | |||||
chrX:153566678
|
A | G | 9 | a0000c0008t0021g0228a0001c0003t0001g0033a0001c0003t0001g0034others(6): Show | 9 | HG01361.hp2 HG02257.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3342+1575A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566678 | ||||||
chrX:153566865
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3342+1762G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566865 | ||||||
chrX:153566884
|
C | G | 3 | a0001c0001t0020g0230a0001c0004t0007g0226a0001c0004t0015g0225 | 3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+1781C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566884 | ||||||
chrX:153566898
|
TC | T | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+1800delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566898 | |||||
chrX:153566908
|
AC | A | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+1807delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566908 | |||||
chrX:153566919
|
G | A | 10 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(7): Show | 11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3342+1816G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566919 | ||||||
chrX:153566963
|
GC | G | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+1866delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153566963 | |||||
chrX:153567023
|
AG | A | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+1922delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567023 | |||||
chrX:153567083
|
AC | A | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+1982delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567083 | |||||
chrX:153567154
|
G | A | 12 | a0001c0001t0001g0111a0001c0001t0001g0217a0001c0001t0004g0014others(9): Show | 13 | HG02027.hp1 NA18612.hp1 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.3342+2051G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567154 | ||||||
chrX:153567163
|
TC | T | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+2064delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567163 | |||||
chrX:153567188
|
GC | G | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+2087delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567188 | |||||
chrX:153567332
|
GC | G | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+2232delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567332 | |||||
chrX:153567367
|
G | GC | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3342+2270dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567367 | |||||
chrX:153567448
|
TG | T | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+2351delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567448 | |||||
chrX:153567482
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3342+2379C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567482 | ||||||
chrX:153567516
|
C | T | 1 | a0001c0001t0046g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3342+2413C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567516 | ||||||
chrX:153567586
|
A | AC | 1 | a0001c0002t0002g0187 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3342+2487dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567586 | |||||
chrX:153567694
|
A | G | 233 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3342+2591A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567694 | ||||||
chrX:153567710
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0121others(3): Show | 6 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.3342+2607G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567710 | ||||||
chrX:153567735
|
T | C | 246 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(243): Show | 264 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.3342+2632T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567735 | ||||||
chrX:153567739
|
G | A | 232 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 249 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.3342+2636G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567739 | ||||||
chrX:153567798
|
C | T | 3 | a0001c0002t0001g0141a0002c0006t0003g0140a0007c0023t0001g0097 | 3 | HG02080.hp2 NA18962.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3342+2695C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567798 | ||||||
chrX:153567818
|
C | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0121others(2): Show | 5 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3342+2715C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567818 | ||||||
chrX:153567840
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0022g0233 | 3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3342+2737A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567840 | ||||||
chrX:153567841
|
T | TC | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+2740dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153567841 | |||||
chrX:153568045
|
C | A | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3342+2942C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568045 | ||||||
chrX:153568046
|
A | C | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3342+2943A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568046 | ||||||
chrX:153568223
|
G | A | 4 | a0000c0008t0021g0228a0001c0001t0001g0027a0001c0001t0001g0030others(1): Show | 4 | HG02965.hp1 HG02976.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3342+3120G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568223 | ||||||
chrX:153568263
|
G | T | 3 | a0001c0001t0020g0230a0001c0004t0007g0226a0001c0004t0015g0225 | 3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+3160G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568263 | ||||||
chrX:153568300
|
C | T | 2 | a0001c0002t0001g0153a0001c0002t0001g0156 | 2 | NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3342+3197C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568300 | ||||||
chrX:153568435
|
A | G | 128 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.3342+3332A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568435 | ||||||
chrX:153568499
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0244 | 2 | HG00609.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.3342+3396C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568499 | ||||||
chrX:153568545
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0022g0233 | 3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3342+3442G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568545 | ||||||
chrX:153568634
|
G | A | 4 | a0001c0002t0012g0087a0001c0002t0012g0088a0001c0002t0012g0089others(1): Show | 4 | NA18948.hp1 NA18998.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+3531G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568634 | ||||||
chrX:153568702
|
G | A | 62 | a0001c0001t0001g0125a0001c0002t0001g0001a0001c0002t0001g0009others(59): Show | 68 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3342+3599G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568702 | ||||||
chrX:153568786
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0112a0001c0001t0001g0158others(3): Show | 6 | HG00423.hp1 HG00558.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+3683C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568786 | ||||||
chrX:153568984
|
C | T | 3 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0165 | 4 | HG02280.hp2 HG02622.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3342+3881C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568984 | ||||||
chrX:153569009
|
C | T | 68 | a0000c0008t0021g0228a0001c0001t0001g0027a0001c0001t0001g0030others(65): Show | 74 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.3342+3906C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569009 | ||||||
chrX:153569158
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3342+4055C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569158 | ||||||
chrX:153569181
|
G | A | 2 | a0001c0002t0001g0116a0001c0002t0001g0216 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.3342+4078G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569181 | ||||||
chrX:153569278
|
T | C | 72 | a0000c0013t0041g0041a0001c0001t0001g0047a0001c0001t0001g0125others(69): Show | 79 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.3342+4175T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569278 | ||||||
chrX:153569312
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3342+4209G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569312 | ||||||
chrX:153569349
|
A | AC | 1 | a0005c0012t0044g0224 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3342+4251dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153569349 | |||||
chrX:153569361
|
TC | T | 2 | a0001c0002t0001g0094a0001c0002t0030g0018 | 2 | NA19063.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.3342+4261delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153569361 | |||||
chrX:153569433
|
G | C | 73 | a0000c0013t0041g0041a0001c0001t0001g0047a0001c0001t0001g0125others(70): Show | 80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3342+4330G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569433 | ||||||
chrX:153569501
|
C | T | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3342+4398C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569501 | ||||||
chrX:153569543
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3342+4440C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569543 | ||||||
chrX:153569764
|
T | C | 3 | a0001c0001t0016g0186a0001c0002t0001g0077a0001c0002t0016g0076 | 3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3342+4661T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569764 | ||||||
chrX:153569843
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3342+4740C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569843 | ||||||
chrX:153570001
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3342+4898G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570001 | ||||||
chrX:153570071
|
T | C | 3 | a0001c0001t0016g0186a0001c0002t0001g0077a0001c0002t0016g0076 | 3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3342+4968T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570071 | ||||||
chrX:153570121
|
T | TG | 8 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.3342+5019dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570121 | |||||
chrX:153570223
|
A | C | 1 | a0001c0003t0052g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3342+5120A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570223 | ||||||
chrX:153570302
|
C | T | 6 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0165others(3): Show | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+5199C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570302 | ||||||
chrX:153570376
|
GC | G | 1 | a0001c0001t0001g0059 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3342+5277delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570376 | |||||
chrX:153570387
|
C | T | 1 | a0001c0001t0049g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5284C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570387 | ||||||
chrX:153570418
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0055 | 2 | NA18979.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.3342+5315C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570418 | ||||||
chrX:153570441
|
G | C | 6 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0165others(3): Show | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+5338G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570441 | ||||||
chrX:153570487
|
A | AT | 2 | a0001c0002t0001g0141a0007c0023t0001g0097 | 2 | NA18962.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3342+5384_3342+538 others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570487 | ||||||
chrX:153570655
|
T | C | 1 | a0001c0002t0002g0196 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3342+5552T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570655 | ||||||
chrX:153570860
|
C | CT | 2 | a0001c0001t0003g0063a0001c0011t0023g0232 | 2 | HG01928.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3342+5768dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570860 | |||||
chrX:153570860
|
CT | C | 4 | a0001c0001t0001g0059a0001c0002t0030g0018a0001c0003t0007g0231others(1): Show | 4 | HG02257.hp2 HG02886.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+5768delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570860 | |||||
chrX:153570917
|
A | G | 1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3342+5814A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570917 | ||||||
chrX:153570962
|
G | A | 1 | a0001c0022t0025g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3342+5859G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570962 | ||||||
chrX:153570995
|
T | TGC | 1 | a0001c0001t0046g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3342+5898_3342+589 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570995 | |||||
chrX:153571002
|
G | A | 1 | a0001c0002t0001g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3342+5899G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | ||||||
chrX:153571002
|
G | GCA | 12 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(9): Show | 12 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3342+5899_3342+590 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | ||||||
chrX:153571002
|
GTACA | G | 3 | a0001c0003t0026g0235a0001c0003t0047g0100a0001c0010t0005g0173 | 3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3342+5900_3342+590 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | ||||||
chrX:153571002
|
GTACACA | G | 4 | a0001c0001t0016g0186a0001c0001t0049g0083a0001c0002t0001g0077others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+5900_3342+590 others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | ||||||
chrX:153571003
|
T | C | 16 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0091others(13): Show | 17 | HG00741.hp1 HG01243.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.3342+5900T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571003 | ||||||
chrX:153571003
|
T | TAC | 80 | a0000c0008t0021g0228a0000c0013t0041g0041a0001c0001t0001g0002others(77): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.3342+5935_3342+593 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
T | TACAC | 63 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0078others(60): Show | 68 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3342+5933_3342+593 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
T | TACACAC | 32 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0062others(29): Show | 32 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.3342+5931_3342+593 others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
T | TACACACA others(1): Show |
11 | a0001c0001t0004g0014a0001c0001t0005g0163a0001c0001t0033g0214others(8): Show | 12 | HG00738.hp1 HG01081.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.3342+5929_3342+593 others(12): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0061a0002c0006t0001g0151 | 2 | HG01123.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.3342+5927_3342+593 others(14): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
TAC | T | 6 | a0001c0001t0001g0161a0001c0001t0001g0206a0001c0001t0001g0208others(3): Show | 6 | HG00639.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+5935_3342+593 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571003
|
TACAC | T | 3 | a0001c0001t0020g0230a0001c0002t0002g0004a0001c0002t0002g0196 | 5 | HG01123.hp2 HG01346.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3342+5933_3342+593 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | |||||
chrX:153571010
|
A | G | 1 | a0001c0001t0049g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5907A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571010 | ||||||
chrX:153571012
|
A | G | 1 | a0001c0001t0049g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5909A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571012 | ||||||
chrX:153571157
|
G | A | 1 | a0001c0001t0014g0064 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3342+6054G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571157 | ||||||
chrX:153571188
|
AG | A | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+6089delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571188 | |||||
chrX:153571220
|
G | A | 4 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0002g0043others(1): Show | 4 | HG03688.hp1 HG03831.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+6117G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571220 | ||||||
chrX:153571263
|
G | A | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3342+6160G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571263 | ||||||
chrX:153571498
|
C | CAGGGGTG others(18): Show |
1 | a0001c0001t0009g0236 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3342+6397_3342+639 others(29): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571498 | |||||
chrX:153571516
|
C | CA | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3342+6414dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571516 | |||||
chrX:153571524
|
GC | G | 1 | a0001c0002t0030g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3342+6424delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571524 | |||||
chrX:153571536
|
T | TG | 1 | a0001c0001t0049g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+6437dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571536 | |||||
chrX:153571586
|
G | A | 1 | a0001c0002t0003g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3342+6483G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571586 | ||||||
chrX:153571690
|
G | A | 4 | a0001c0002t0001g0098a0001c0002t0001g0129a0001c0002t0017g0103others(1): Show | 4 | HG00639.hp2 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+6587G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571690 | ||||||
chrX:153571792
|
G | A | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0121others(4): Show | 7 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+6689G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571792 | ||||||
chrX:153571828
|
GC | G | 1 | a0001c0001t0015g0227 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3342+6728delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571828 | |||||
chrX:153571992
|
T | C | 1 | a0004c0019t0001g0114 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3342+6889T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571992 | ||||||
chrX:153572247
|
C | T | 33 | a0001c0001t0002g0021a0001c0001t0002g0164a0001c0001t0009g0236others(30): Show | 35 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.3342+7144C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572247 | ||||||
chrX:153572273
|
G | A | 39 | a0001c0001t0002g0021a0001c0001t0002g0164a0001c0001t0008g0013others(36): Show | 42 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3342+7170G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572273 | ||||||
chrX:153572385
|
G | A | 6 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+7282G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572385 | ||||||
chrX:153572628
|
CAT | C | 246 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(243): Show | 264 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.3343-7347_3343-734 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153572628 | |||||
chrX:153572649
|
T | C | 17 | a0000c0008t0021g0228a0001c0001t0001g0027a0001c0001t0001g0030others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3343-7329T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572649 | ||||||
chrX:153572663
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-7315C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572663 | ||||||
chrX:153572867
|
A | AG | 1 | a0001c0001t0002g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3343-7106dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153572867 | |||||
chrX:153572896
|
A | T | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-7082A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572896 | ||||||
chrX:153572966
|
A | G | 1 | a0001c0001t0022g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3343-7012A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572966 | ||||||
chrX:153573216
|
T | G | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-6762T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573216 | ||||||
chrX:153573267
|
G | A | 39 | a0001c0001t0002g0021a0001c0001t0002g0164a0001c0001t0008g0013others(36): Show | 42 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3343-6711G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573267 | ||||||
chrX:153573311
|
G | A | 44 | a0001c0001t0002g0021a0001c0001t0002g0039a0001c0001t0002g0055others(41): Show | 47 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.3343-6667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573311 | ||||||
chrX:153573339
|
G | A | 4 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-6639G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573339 | ||||||
chrX:153573377
|
T | C | 1 | a0001c0002t0001g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3343-6601T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573377 | ||||||
chrX:153573575
|
A | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0011g0036others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-6403A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573575 | ||||||
chrX:153573654
|
G | A | 71 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0001g0120others(68): Show | 77 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.3343-6324G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573654 | ||||||
chrX:153573680
|
T | A | 142 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0027others(139): Show | 151 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.3343-6298T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573680 | ||||||
chrX:153573783
|
G | A | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-6195G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573783 | ||||||
chrX:153573948
|
C | G | 132 | a0000c0018t0013g0090a0001c0001t0001g0047a0001c0001t0001g0117others(129): Show | 141 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.3343-6030C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573948 | ||||||
chrX:153573969
|
G | A | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3343-6009G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573969 | ||||||
chrX:153574000
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3343-5978C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574000 | ||||||
chrX:153574011
|
T | C | 131 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0047others(128): Show | 140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.3343-5967T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574011 | ||||||
chrX:153574025
|
G | T | 135 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0047others(132): Show | 144 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3343-5953G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574025 | ||||||
chrX:153574239
|
C | T | 13 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0035others(10): Show | 13 | HG00741.hp1 HG01243.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3343-5739C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574239 | ||||||
chrX:153574363
|
G | C | 1 | a0001c0002t0001g0141 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3343-5615G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574363 | ||||||
chrX:153574424
|
G | A | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-5554G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574424 | ||||||
chrX:153574493
|
T | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0011g0036others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-5485T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574493 | ||||||
chrX:153574863
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3343-5115G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574863 | ||||||
chrX:153574909
|
T | TC | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3343-5068dupC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153574909 | |||||
chrX:153574949
|
A | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0011g0036others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3343-5029A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574949 | ||||||
chrX:153575124
|
G | A | 42 | a0001c0001t0002g0021a0001c0001t0002g0039a0001c0001t0002g0055others(39): Show | 45 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.3343-4854G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575124 | ||||||
chrX:153575150
|
C | T | 1 | a0001c0001t0020g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-4828C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575150 | ||||||
chrX:153575248
|
G | A | 1 | a0001c0002t0010g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3343-4730G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575248 | ||||||
chrX:153575570
|
C | T | 2 | a0001c0007t0001g0046a0001c0007t0001g0069 | 2 | NA18944.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3343-4408C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575570 | ||||||
chrX:153575638
|
G | A | 3 | a0001c0001t0016g0186a0001c0002t0001g0077a0001c0002t0016g0076 | 3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3343-4340G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575638 | ||||||
chrX:153575765
|
C | T | 1 | a0001c0002t0010g0102 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3343-4213C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575765 | ||||||
chrX:153575840
|
T | TG | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3343-4133dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153575840 | |||||
chrX:153575863
|
A | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0011g0036others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-4115A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575863 | ||||||
chrX:153575906
|
A | AG | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3343-4071dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153575906 | |||||
chrX:153575991
|
G | A | 1 | a0001c0001t0006g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3343-3987G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575991 | ||||||
chrX:153576026
|
A | T | 1 | a0001c0002t0002g0192 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3343-3952A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576026 | ||||||
chrX:153576034
|
C | T | 1 | a0001c0001t0051g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3343-3944C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576034 | ||||||
chrX:153576058
|
CT | C | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3343-3915delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153576058 | |||||
chrX:153576274
|
T | A | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-3704T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576274 | ||||||
chrX:153576283
|
A | AG | 1 | a0001c0002t0001g0179 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3343-3692dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153576283 | |||||
chrX:153576501
|
C | T | 1 | a0001c0002t0001g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3343-3477C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576501 | ||||||
chrX:153576552
|
G | A | 73 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0001g0120others(70): Show | 79 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.3343-3426G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576552 | ||||||
chrX:153576683
|
TG | T | 1 | a0001c0002t0001g0094 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3343-3292delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153576683 | |||||
chrX:153576893
|
T | C | 2 | a0001c0001t0009g0236a0001c0003t0002g0085 | 2 | HG00642.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3343-3085T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576893 | ||||||
chrX:153576919
|
C | G | 4 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-3059C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576919 | ||||||
chrX:153577093
|
C | T | 2 | a0001c0002t0017g0103a0001c0002t0017g0201 | 2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.3343-2885C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577093 | ||||||
chrX:153577094
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3343-2884G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577094 | ||||||
chrX:153577174
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3343-2804C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577174 | ||||||
chrX:153577209
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0022g0233others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3343-2769T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577209 | ||||||
chrX:153577283
|
G | C | 72 | a0001c0001t0001g0047a0001c0001t0001g0117a0001c0001t0001g0120others(69): Show | 78 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.3343-2695G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577283 | ||||||
chrX:153577284
|
T | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0022g0233others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3343-2694T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577284 | ||||||
chrX:153577463
|
T | TG | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3343-2512dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153577463 | |||||
chrX:153577529
|
C | T | 14 | a0000c0018t0013g0090a0001c0001t0002g0184a0001c0001t0005g0035others(11): Show | 14 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3343-2449C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577529 | ||||||
chrX:153577669
|
G | A | 46 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0217others(43): Show | 52 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3343-2309G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577669 | ||||||
chrX:153577705
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3343-2273G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577705 | ||||||
chrX:153577721
|
C | T | 1 | a0001c0002t0002g0194 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3343-2257C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577721 | ||||||
chrX:153577867
|
G | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0011g0036others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3343-2111G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577867 | ||||||
chrX:153577871
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0177others(1): Show | 4 | HG00735.hp2 HG01069.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-2107C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577871 | ||||||
chrX:153577899
|
C | T | 88 | a0000c0008t0021g0228a0000c0018t0013g0090a0001c0001t0001g0047others(85): Show | 94 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.3343-2079C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577899 | ||||||
chrX:153577932
|
T | C | 4 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-2046T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577932 | ||||||
chrX:153577957
|
G | C | 1 | a0003c0009t0005g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3343-2021G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577957 | ||||||
chrX:153578189
|
GC | G | 4 | a0001c0001t0011g0036a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-1785delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153578189 | |||||
chrX:153578518
|
G | C | 7 | a0001c0002t0002g0012a0001c0002t0002g0044a0001c0002t0002g0188others(4): Show | 7 | HG00423.hp2 HG01433.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.3343-1460G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578518 | ||||||
chrX:153578615
|
A | C | 140 | a0000c0008t0021g0228a0000c0013t0041g0041a0000c0018t0013g0090others(137): Show | 149 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.3343-1363A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578615 | ||||||
chrX:153578638
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3343-1340G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578638 | ||||||
chrX:153578653
|
T | G | 1 | a0001c0001t0011g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3343-1325T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578653 | ||||||
chrX:153578658
|
C | T | 1 | a0001c0002t0003g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3343-1320C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578658 | ||||||
chrX:153578697
|
G | A | 3 | a0001c0003t0007g0231a0001c0003t0034g0029a0001c0022t0025g0234 | 3 | HG02257.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3343-1281G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578697 | ||||||
chrX:153578701
|
T | C | 1 | a0001c0001t0049g0083 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3343-1277T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578701 | ||||||
chrX:153578715
|
G | T | 1 | a0001c0002t0029g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3343-1263G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578715 | ||||||
chrX:153578772
|
G | C | 3 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0165 | 4 | HG02280.hp2 HG02622.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3343-1206G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578772 | ||||||
chrX:153578777
|
A | G | 86 | a0000c0008t0021g0228a0001c0001t0001g0027a0001c0001t0001g0030others(83): Show | 92 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.3343-1201A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578777 | ||||||
chrX:153578792
|
T | C | 75 | a0000c0008t0021g0228a0001c0001t0001g0047a0001c0001t0001g0111others(72): Show | 81 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.3343-1186T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578792 | ||||||
chrX:153578859
|
A | G | 4 | a0000c0008t0021g0228a0001c0001t0020g0230a0001c0001t0049g0083others(1): Show | 4 | HG01934.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3343-1119A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578859 | ||||||
chrX:153578866
|
G | A | 149 | a0000c0013t0041g0041a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 161 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.3343-1112G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578866 | ||||||
chrX:153578901
|
G | A | 2 | a0000c0008t0021g0228a0001c0003t0002g0211 | 2 | HG01934.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3343-1077G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578901 | ||||||
chrX:153578915
|
A | ACAGGGGC others(7): Show |
1 | a0000c0008t0021g0228 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3343-1059_3343-104 others(18): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153578915 | |||||
chrX:153578950
|
T | C | 1 | a0001c0020t0009g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3343-1028T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578950 | ||||||
chrX:153578952
|
C | T | 2 | a0001c0001t0009g0236a0001c0003t0002g0085 | 2 | HG00642.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3343-1026C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578952 | ||||||
chrX:153579091
|
T | C | 81 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0047others(78): Show | 87 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.3343-887T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579091 | ||||||
chrX:153579260
|
G | A | 6 | a0000c0008t0021g0228a0001c0001t0020g0230a0001c0001t0027g0240others(3): Show | 6 | HG01934.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3343-718G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579260 | ||||||
chrX:153579347
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3343-631G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579347 | ||||||
chrX:153579509
|
CT | C | 1 | a0001c0001t0004g0040 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3343-465delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153579509 | |||||
chrX:153579619
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3343-359C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579619 | ||||||
chrX:153579716
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0078others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-262C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579716 | ||||||
chrX:153579736
|
GA | G | 2 | a0001c0001t0027g0240a0001c0001t0051g0017 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-238delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153579736 | |||||
chrX:153579833
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0078others(8): Show | 11 | HG01934.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3343-145C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579833 | ||||||
chrX:153579834
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3343-144G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579834 |