geneid | 27032 |
---|---|
ensemblid | ENSG00000017260.20 |
hgncid | 13211 |
symbol | ATP2C1 |
name | ATPase secretory pathway Ca2+ transporting 1 |
refseq_nuc | NM_001378687.1 |
refseq_prot | NP_001365616.1 |
ensembl_nuc | ENST00000510168.6 |
ensembl_prot | ENSP00000427461.1 |
mane_status | MANE Select |
chr | chr3 |
start | 130894084 |
end | 131003150 |
strand | + |
ver | v1.2 |
region | chr3:130894084-131003150 |
region5000 | chr3:130889084-131008150 |
regionname0 | ATP2C1_chr3_130894084_131003150 |
regionname5000 | ATP2C1_chr3_130889084_131008150 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 919 | 374 | 83 | 60 | 181 | 14 | 34 | 143 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0002 | 0/0 | 919 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0003 | 0/0 | 919 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0004 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0005 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2760 | 326 | 77 | 54 | 153 | 13 | 27 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0002 | 0/0 | 2760 | 39 | 0 | 4 | 27 | 1 | 7 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0003 | 0/0 | 2760 | 7 | 5 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0004 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0005 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0006 | 0/0 | 2760 | 2 | 1 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0007 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
c0008 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2235 | 366 | 83 | 59 | 175 | 14 | 33 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0002 | 0/0 | 2230 | 4 | 3 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0003 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0004 | 0/0 | 2235 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0005 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0006 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0007 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0008 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0009 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0010 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0011 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
t0012 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2760 | 326 | 77 | 54 | 153 | 13 | 27 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0002 | 0/0 | 2760 | 39 | 0 | 4 | 27 | 1 | 7 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0003 | 0/0 | 2760 | 7 | 5 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0006 | 0/0 | 2760 | 2 | 1 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0002c0004 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0003c0005 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0004c0007 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0005c0008 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4994 | 313 | 72 | 53 | 147 | 13 | 26 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0002 | 0/0 | 4989 | 4 | 3 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0004 | 0/0 | 4994 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0005 | 0/0 | 4994 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0006 | 0/0 | 4994 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0007 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0009 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0010 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0011 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0001t0012 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0002t0001 | 0/0 | 4994 | 38 | 0 | 4 | 26 | 1 | 7 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0002t0008 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0003t0001 | 0/0 | 4994 | 7 | 5 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0001c0006t0001 | 0/0 | 4994 | 2 | 1 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0002c0004t0001 | 0/0 | 4994 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0003c0005t0003 | 0/0 | 4994 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0004c0007t0001 | 0/0 | 4994 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
a0005c0008t0001 | 0/0 | 4994 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | copy fasta | chr3 | 130889084 | 131008150 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0011g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0002t0008g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0003t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0001c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0002c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0002c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0002c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0002c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0003c0005t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0003c0005t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0004c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
a0005c0008t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0367 | EUR | FIN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00558 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0369 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0172 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0375 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0231 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0363 | EUR | IBS | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0346 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CDX | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0374 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02280 | hp1 | a0001 | c0006 | t0001 | g0111 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0342 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0098 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0076 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0097 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02723 | hp2 | a0005 | c0008 | t0001 | g0193 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0344 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0371 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0370 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0372 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02970 | hp1 | a0003 | c0005 | t0003 | g0100 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03041 | hp2 | a0002 | c0004 | t0001 | g0096 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0099 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0110 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0326 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0345 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0351 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0335 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0376 | SAS | BEB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | STU | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | CHB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18966 | hp2 | a0001 | c0001 | t0011 | g0283 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18973 | hp2 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19030 | hp2 | a0003 | c0005 | t0003 | g0101 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19072 | hp1 | a0004 | c0007 | t0001 | g0198 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19088 | hp2 | a0001 | c0006 | t0001 | g0263 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19090 | hp2 | a0001 | c0002 | t0008 | g0327 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0362 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0373 | AFR | MSL | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0234 | REF | REF | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | ATP2C1_chr3_130889084_131008150 | ATP2C1 | chr3 | 130889084 | 131008150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:130955015
|
G | A | 1 | a0003 | 2 | HG02970.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.691G>A | p.Val231Ile | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/28 | 1125/4994 | 691/2760 | 231/919 | chr3 | 130955015 | ||
chr3:130969331
|
G | A | 1 | a0002 | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.1348G>A | p.Ala450Thr | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/28 | 1782/4994 | 1348/2760 | 450/919 | chr3 | 130969331 | ||
chr3:130969337
|
T | C | 1 | a0004 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.1354T>C | p.Tyr452His | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/28 | 1788/4994 | 1354/2760 | 452/919 | chr3 | 130969337 | ||
chr3:130979301
|
G | C | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1623G>C | p.Leu541Phe | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/28 | 2057/4994 | 1623/2760 | 541/919 | chr3 | 130979301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:130953925
|
G | A | 1 | a0001c0003 | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.636G>A | p.Ser212Ser | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/28 | 1070/4994 | 636/2760 | 212/919 | chr3 | 130953925 | ||
chr3:130959276
|
A | G | 1 | a0003c0005 | 2 | HG02970.hp1 NA19030.hp2 |
splice_region_variant&synonymous_variant | LOW | c.834A>G | p.Gly278Gly | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/28 | 1268/4994 | 834/2760 | 278/919 | chr3 | 130959276 | ||
chr3:130979361
|
C | T | 1 | a0001c0006 | 2 | HG02280.hp1 NA19088.hp2 |
synonymous_variant | LOW | c.1683C>T | p.Ala561Ala | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/28 | 2117/4994 | 1683/2760 | 561/919 | chr3 | 130979361 | ||
chr3:130999628
|
G | A | 1 | a0001c0002 | 39 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(36): Show |
synonymous_variant | LOW | c.2598G>A | p.Lys866Lys | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/28 | 3032/4994 | 2598/2760 | 866/919 | chr3 | 130999628 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:130894172
|
C | T | 1 | a0001c0001t0004 | 2 | HG00544.hp2 HG02015.hp2 |
5_prime_UTR_variant | MODIFIER | c.-346C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 598 | chr3 | 130894172 | |||||
chr3:130894190
|
C | A | 1 | a0001c0001t0005 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-328C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 580 | chr3 | 130894190 | |||||
chr3:130894195
|
G | T | 1 | a0001c0001t0012 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-323G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 575 | chr3 | 130894195 | |||||
chr3:130894218
|
G | A | 1 | a0001c0001t0006 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-300G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 552 | chr3 | 130894218 | |||||
chr3:130894310
|
C | A | 1 | a0001c0001t0007 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-208C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/28 | 460 | chr3 | 130894310 | |||||
chr3:130894717
|
G | C | 1 | a0001c0002t0008 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/28 | 53 | chr3 | 130894717 | |||||
chr3:131001596
|
G | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 246 | chr3 | 131001596 | |||||
chr3:131001597
|
G | T | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 247 | chr3 | 131001597 | |||||
chr3:131001598
|
T | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*248T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 248 | chr3 | 131001598 | |||||
chr3:131001599
|
C | A | 1 | a0001c0001t0009 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 249 | chr3 | 131001599 | |||||
chr3:131001842
|
TTGTAA | T | 1 | a0001c0001t0002 | 4 | HG02970.hp2 HG02976.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*498_*502delTGTAA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 498 | INFO_REALIGN_3_PRIME | chr3 | 131001842 | ||||
chr3:131002036
|
G | A | 1 | a0001c0001t0010 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 686 | chr3 | 131002036 | |||||
chr3:131002281
|
C | G | 1 | a0001c0001t0011 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*931C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 931 | chr3 | 131002281 | |||||
chr3:131002895
|
A | G | 1 | a0003c0005t0003 | 2 | HG02970.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1545A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 28/28 | 1545 | chr3 | 131002895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:130894512
|
GCTCCCGA others(20): Show |
G | 1 | a0001c0002t0001g0376 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-180-73_-180-47del others(27): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr3 | 130894512 | |||||
chr3:130894533
|
C | T | 7 | a0001c0003t0001g0369a0001c0003t0001g0370a0001c0003t0001g0371others(4): Show | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-57C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 1/27 | chr3 | 130894533 | ||||||
chr3:130894790
|
C | G | 9 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+15C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130894790 | ||||||
chr3:130895069
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.6+294G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895069 | ||||||
chr3:130895186
|
G | C | 1 | a0001c0002t0001g0008 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.6+411G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895186 | ||||||
chr3:130895306
|
C | G | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.6+531C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895306 | ||||||
chr3:130895350
|
C | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.6+575C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895350 | ||||||
chr3:130895564
|
G | T | 1 | a0001c0001t0001g0314 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6+789G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895564 | ||||||
chr3:130895667
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.6+892T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895667 | ||||||
chr3:130895809
|
C | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.6+1034C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130895809 | ||||||
chr3:130895964
|
AT | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+1192delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130895964 | |||||
chr3:130896099
|
A | T | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6+1324A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896099 | ||||||
chr3:130896298
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6+1523G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896298 | ||||||
chr3:130896787
|
T | C | 1 | a0001c0003t0001g0369 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6+2012T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896787 | ||||||
chr3:130896820
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+2045G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896820 | ||||||
chr3:130896908
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG00639.hp1 HG01258.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2133G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896908 | ||||||
chr3:130896998
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6+2223G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130896998 | ||||||
chr3:130897044
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6+2269G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897044 | ||||||
chr3:130897117
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6+2342C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897117 | ||||||
chr3:130897170
|
A | T | 37 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+2395A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897170 | ||||||
chr3:130897371
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6+2596T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897371 | ||||||
chr3:130897382
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.6+2607C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897382 | ||||||
chr3:130897728
|
G | A | 7 | a0001c0003t0001g0369a0001c0003t0001g0370a0001c0003t0001g0371others(4): Show | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+2953G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897728 | ||||||
chr3:130897747
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6+2972G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897747 | ||||||
chr3:130897849
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6+3074G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130897849 | ||||||
chr3:130898290
|
A | T | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+3515A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898290 | ||||||
chr3:130898409
|
G | C | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+3634G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898409 | ||||||
chr3:130898429
|
T | C | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.6+3654T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898429 | ||||||
chr3:130898439
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(8): Show | 12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+3664T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898439 | ||||||
chr3:130898623
|
A | C | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+3848A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898623 | ||||||
chr3:130898728
|
C | T | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+3953C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898728 | ||||||
chr3:130898847
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6+4072G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898847 | ||||||
chr3:130898936
|
A | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+4161A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898936 | ||||||
chr3:130898993
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+4218G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130898993 | ||||||
chr3:130899362
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+4587A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899362 | ||||||
chr3:130899618
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6+4843C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899618 | ||||||
chr3:130899680
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6+4905A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899680 | ||||||
chr3:130899858
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+5083T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899858 | ||||||
chr3:130899877
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+5102A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899877 | ||||||
chr3:130899954
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6+5179A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130899954 | ||||||
chr3:130900015
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+5240C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900015 | ||||||
chr3:130900536
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6+5761A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900536 | ||||||
chr3:130900870
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02451.hp2 HG02630.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+6095A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130900870 | ||||||
chr3:130901005
|
T | C | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+6230T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901005 | ||||||
chr3:130901012
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6+6237G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901012 | ||||||
chr3:130901366
|
T | C | 32 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.6+6591T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901366 | ||||||
chr3:130901376
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6+6601C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901376 | ||||||
chr3:130901866
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+7091C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901866 | ||||||
chr3:130901917
|
G | A | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+7142G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901917 | ||||||
chr3:130901948
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+7173A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901948 | ||||||
chr3:130901964
|
A | G | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.6+7189A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130901964 | ||||||
chr3:130902008
|
C | T | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+7233C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902008 | ||||||
chr3:130902114
|
T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0173others(20): Show | 24 | HG00544.hp1 HG00558.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.6+7339T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902114 | ||||||
chr3:130902283
|
CGTTTTTT others(6): Show |
C | 29 | a0001c0001t0001g0002a0001c0001t0001g0075a0001c0001t0001g0081others(26): Show | 30 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.6+7522_6+7534delGT others(11): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902283 | |||||
chr3:130902284
|
G | GT | 12 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0117others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+7521dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
G | GTT | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG00741.hp2 HG04184.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+7520_6+7521dupTT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
G | GTTTTTTT others(3): Show |
1 | a0001c0003t0001g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6+7512_6+7521dupTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
G | GTTTTTTT others(9): Show |
1 | a0001c0003t0001g0375 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6+7521_6+7522insTT others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
G | GTTTTTTT others(16): Show |
1 | a0001c0003t0001g0369 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6+7521_6+7522insTT others(21): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(7): Show |
G | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 94 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.6+7522_6+7535delGT others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(8): Show |
G | 24 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0141others(21): Show | 24 | HG01081.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.6+7522_6+7536delGT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(9): Show |
G | 73 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.6+7522_6+7537delGT others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6+7522_6+7538delGT others(15): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0001g0088a0001c0001t0001g0311 | 2 | HG01891.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.6+7522_6+7539delGT others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(12): Show |
G | 35 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(32): Show | 35 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.6+7522_6+7540delGT others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+7522_6+7541delGT others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902284
|
GTTTTTTT others(15): Show |
G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.6+7522_6+7543delGT others(20): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902284 | |||||
chr3:130902285
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0001g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6+7522_6+7533delGT others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902285 | |||||
chr3:130902287
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0001g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.6+7522_6+7531delGT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902287 | |||||
chr3:130902291
|
T | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+7516T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902291 | ||||||
chr3:130902296
|
TG | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0136others(2): Show | 5 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+7522delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902296 | ||||||
chr3:130902297
|
G | GT | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+7547dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902297 | |||||
chr3:130902297
|
G | T | 32 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(29): Show | 32 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.6+7522G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902297 | ||||||
chr3:130902298
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.6+7523T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902298 | ||||||
chr3:130902300
|
T | G | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+7525T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902300 | ||||||
chr3:130902310
|
T | G | 2 | a0001c0001t0001g0275a0001c0001t0006g0110 | 2 | HG03491.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.6+7535T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902310 | ||||||
chr3:130902312
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+7537T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902312 | ||||||
chr3:130902346
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+7571G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902346 | ||||||
chr3:130902370
|
T | G | 19 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(16): Show | 19 | HG00609.hp1 HG02056.hp2 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.6+7595T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902370 | ||||||
chr3:130902547
|
C | CATTTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+7775_6+7779dupTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130902547 | |||||
chr3:130902637
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 8 | HG02717.hp2 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+7862T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902637 | ||||||
chr3:130902657
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.6+7882C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902657 | ||||||
chr3:130902786
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.6+8011G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902786 | ||||||
chr3:130902859
|
G | A | 49 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.6+8084G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130902859 | ||||||
chr3:130903442
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6+8667G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903442 | ||||||
chr3:130903504
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.6+8729G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903504 | ||||||
chr3:130903611
|
T | C | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+8836T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903611 | ||||||
chr3:130903613
|
C | T | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+8838C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903613 | ||||||
chr3:130903686
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.6+8911C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903686 | ||||||
chr3:130903688
|
A | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(35): Show | 39 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.6+8913A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903688 | ||||||
chr3:130903693
|
CCCTTTCC others(5): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6+8926_6+8937delCC others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903693 | |||||
chr3:130903700
|
C | CCCTTT | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(11): Show | 14 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+8958_6+8962dupTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(3): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+8953_6+8962dupTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(8): Show |
2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.6+8948_6+8962dupTT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(13): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 6 | HG02818.hp2 HG02895.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+8943_6+8962dupTT others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(18): Show |
4 | a0001c0001t0001g0083a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG01884.hp2 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+8938_6+8962dupTT others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(23): Show |
1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6+8933_6+8962dupTT others(28): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
C | CCCTTTCC others(28): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.6+8928_6+8962dupTT others(33): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
CCCTTT | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.6+8958_6+8962delTT others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
CCCTTTCC others(3): Show |
C | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6+8953_6+8962delTT others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903700
|
CCCTTTCC others(8): Show |
C | 1 | a0001c0002t0001g0315 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.6+8948_6+8962delTT others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130903700 | |||||
chr3:130903741
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6+8966T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130903741 | ||||||
chr3:130904496
|
T | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0209others(4): Show | 7 | NA18978.hp2 NA18988.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+9721T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130904496 | ||||||
chr3:130904734
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+9959A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130904734 | ||||||
chr3:130905227
|
G | A | 42 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(39): Show | 42 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.6+10452G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905227 | ||||||
chr3:130905462
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | NA18946.hp1 NA18964.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+10687A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905462 | ||||||
chr3:130905572
|
C | G | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+10797C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905572 | ||||||
chr3:130905706
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+10931A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905706 | ||||||
chr3:130905739
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+10964A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905739 | ||||||
chr3:130905861
|
T | C | 7 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0209others(4): Show | 7 | NA18978.hp2 NA18988.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+11086T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905861 | ||||||
chr3:130905951
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(8): Show | 12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+11176C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905951 | ||||||
chr3:130905990
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.6+11215C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130905990 | ||||||
chr3:130906002
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6+11227A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906002 | ||||||
chr3:130906015
|
T | A | 37 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.6+11240T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906015 | ||||||
chr3:130906122
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+11347A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906122 | ||||||
chr3:130906162
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6+11387T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906162 | ||||||
chr3:130906230
|
C | A | 1 | a0005c0008t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+11455C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906230 | ||||||
chr3:130906437
|
G | C | 10 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(7): Show | 10 | HG02027.hp1 HG02735.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.6+11662G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906437 | ||||||
chr3:130906521
|
T | C | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.6+11746T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906521 | ||||||
chr3:130906575
|
G | A | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6+11800G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906575 | ||||||
chr3:130906675
|
G | GT | 97 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(94): Show | 97 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.6+11916dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130906675 | |||||
chr3:130906675
|
GT | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+11916delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130906675 | |||||
chr3:130906861
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+12086C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906861 | ||||||
chr3:130906944
|
C | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.6+12169C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130906944 | ||||||
chr3:130907079
|
T | TAC | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0081others(70): Show | 75 | HG00408.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.6+12326_6+12327dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | |||||
chr3:130907079
|
T | TACAC | 11 | a0001c0001t0001g0088a0001c0001t0001g0102a0001c0001t0001g0313others(8): Show | 11 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.6+12324_6+12327dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | |||||
chr3:130907079
|
TAC | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+12326_6+12327del others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907079 | |||||
chr3:130907080
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12305A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907080 | ||||||
chr3:130907081
|
C | T | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12306C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907081 | ||||||
chr3:130907103
|
T | C | 1 | a0001c0002t0001g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6+12328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907103 | ||||||
chr3:130907217
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6+12442T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907217 | ||||||
chr3:130907252
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.6+12477C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907252 | ||||||
chr3:130907377
|
A | G | 1 | a0001c0002t0001g0376 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6+12602A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907377 | ||||||
chr3:130907487
|
G | C | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+12712G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907487 | ||||||
chr3:130907591
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6+12816A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907591 | ||||||
chr3:130907722
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+12947C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907722 | ||||||
chr3:130907730
|
C | CT | 34 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(31): Show | 34 | HG00140.hp1 HG00639.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.6+12969dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130907730 | |||||
chr3:130907817
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+13042A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907817 | ||||||
chr3:130907919
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6+13144A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130907919 | ||||||
chr3:130908204
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6+13429C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908204 | ||||||
chr3:130908434
|
G | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.6+13659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908434 | ||||||
chr3:130908469
|
T | TA | 25 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(22): Show | 25 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+13706dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130908469 | |||||
chr3:130908469
|
TA | T | 56 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.6+13706delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130908469 | |||||
chr3:130908470
|
A | T | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+13695A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908470 | ||||||
chr3:130908559
|
C | G | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+13784C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908559 | ||||||
chr3:130908564
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+13789C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908564 | ||||||
chr3:130908597
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+13822C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130908597 | ||||||
chr3:130909318
|
T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6+14543T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909318 | ||||||
chr3:130909383
|
T | C | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+14608T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909383 | ||||||
chr3:130909406
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6+14631C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909406 | ||||||
chr3:130909862
|
T | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0314 | 3 | HG01069.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.6+15087T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909862 | ||||||
chr3:130909877
|
T | A | 1 | a0001c0001t0001g0217 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6+15102T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130909877 | ||||||
chr3:130910043
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6+15268G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910043 | ||||||
chr3:130910070
|
G | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01255.hp1 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.6+15295G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910070 | ||||||
chr3:130910175
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+15400C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910175 | ||||||
chr3:130910496
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+15721T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910496 | ||||||
chr3:130910498
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6+15723G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910498 | ||||||
chr3:130910567
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+15792T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910567 | ||||||
chr3:130910597
|
C | T | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+15822C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910597 | ||||||
chr3:130910626
|
A | G | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6+15851A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910626 | ||||||
chr3:130910659
|
C | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.6+15884C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910659 | ||||||
chr3:130910762
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+15987G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910762 | ||||||
chr3:130910790
|
G | A | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6+16015G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910790 | ||||||
chr3:130910921
|
T | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.6+16146T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910921 | ||||||
chr3:130910931
|
C | T | 1 | a0001c0002t0001g0343 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6+16156C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130910931 | ||||||
chr3:130911026
|
G | C | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6+16251G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911026 | ||||||
chr3:130911056
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.6+16281T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911056 | ||||||
chr3:130911180
|
C | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 309 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.6+16405C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911180 | ||||||
chr3:130911199
|
T | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6+16424T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911199 | ||||||
chr3:130911326
|
G | C | 30 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(27): Show | 30 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.6+16551G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911326 | ||||||
chr3:130911480
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6+16705G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911480 | ||||||
chr3:130911641
|
A | G | 2 | a0001c0002t0001g0341a0001c0002t0001g0353 | 2 | NA18984.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6+16866A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911641 | ||||||
chr3:130911896
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6+17121T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130911896 | ||||||
chr3:130912052
|
T | C | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.6+17277T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912052 | ||||||
chr3:130912237
|
A | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+17462A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912237 | ||||||
chr3:130912243
|
T | C | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+17468T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912243 | ||||||
chr3:130912256
|
T | A | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6+17481T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912256 | ||||||
chr3:130912259
|
A | C | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6+17484A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912259 | ||||||
chr3:130912360
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6+17585A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912360 | ||||||
chr3:130912396
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+17621C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912396 | ||||||
chr3:130912406
|
GA | G | 8 | a0001c0001t0010g0112a0001c0003t0001g0369a0001c0003t0001g0370others(5): Show | 8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.6+17638delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130912406 | |||||
chr3:130912568
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.6+17793A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912568 | ||||||
chr3:130912587
|
A | C | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6+17812A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912587 | ||||||
chr3:130912609
|
G | A | 1 | a0001c0002t0008g0327 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7-17807G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912609 | ||||||
chr3:130912707
|
G | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0127 | 3 | HG00597.hp1 NA19000.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.7-17709G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912707 | ||||||
chr3:130912806
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-17610A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912806 | ||||||
chr3:130912855
|
A | G | 2 | a0001c0001t0002g0115a0001c0001t0012g0123 | 2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-17561A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912855 | ||||||
chr3:130912858
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.7-17558G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130912858 | ||||||
chr3:130913024
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG00639.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.7-17392A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913024 | ||||||
chr3:130913058
|
C | T | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.7-17358C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913058 | ||||||
chr3:130913260
|
AT | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0155a0001c0001t0001g0167 | 3 | NA19011.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.7-17153delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130913260 | |||||
chr3:130913263
|
T | A | 48 | a0001c0001t0001g0059a0001c0001t0001g0089a0001c0001t0001g0090others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.7-17153T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913263 | ||||||
chr3:130913264
|
A | T | 1 | a0001c0002t0001g0343 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7-17152A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913264 | ||||||
chr3:130913314
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7-17102C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913314 | ||||||
chr3:130913417
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-16999G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913417 | ||||||
chr3:130913536
|
C | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-16880C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913536 | ||||||
chr3:130913546
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-16870G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913546 | ||||||
chr3:130913549
|
A | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.7-16867A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913549 | ||||||
chr3:130913568
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7-16848G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913568 | ||||||
chr3:130913647
|
T | A | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-16769T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913647 | ||||||
chr3:130913665
|
C | T | 2 | a0001c0001t0004g0308a0001c0001t0004g0309 | 2 | HG00544.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.7-16751C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913665 | ||||||
chr3:130913846
|
G | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-16570G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913846 | ||||||
chr3:130913873
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7-16543T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130913873 | ||||||
chr3:130914159
|
CT | C | 52 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.7-16248delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914159 | |||||
chr3:130914209
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7-16207A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914209 | ||||||
chr3:130914211
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-16205C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914211 | ||||||
chr3:130914224
|
A | AT | 31 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(28): Show | 31 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-16191dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914224 | |||||
chr3:130914319
|
G | A | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-16097G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914319 | ||||||
chr3:130914323
|
G | GT | 7 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-16083dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130914323 | |||||
chr3:130914457
|
C | T | 8 | a0001c0001t0010g0112a0001c0003t0001g0369a0001c0003t0001g0370others(5): Show | 8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-15959C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914457 | ||||||
chr3:130914458
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-15958C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914458 | ||||||
chr3:130914470
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7-15946A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914470 | ||||||
chr3:130914598
|
T | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.7-15818T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914598 | ||||||
chr3:130914952
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-15464C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914952 | ||||||
chr3:130914962
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7-15454G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130914962 | ||||||
chr3:130915086
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | NA18978.hp2 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.7-15330C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915086 | ||||||
chr3:130915090
|
G | GT | 11 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0116others(8): Show | 11 | HG01175.hp2 HG01358.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.7-15314dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130915090 | |||||
chr3:130915090
|
GT | G | 11 | a0001c0001t0001g0077a0001c0001t0001g0142a0001c0001t0001g0223others(8): Show | 11 | HG00741.hp2 HG01123.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.7-15314delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130915090 | |||||
chr3:130915102
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.7-15314T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915102 | ||||||
chr3:130915135
|
C | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-15281C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915135 | ||||||
chr3:130915197
|
G | A | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-15219G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915197 | ||||||
chr3:130915348
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-15068A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915348 | ||||||
chr3:130915427
|
T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7-14989T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915427 | ||||||
chr3:130915454
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7-14962A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915454 | ||||||
chr3:130915461
|
G | A | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG00735.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-14955G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915461 | ||||||
chr3:130915528
|
T | C | 8 | a0001c0001t0010g0112a0001c0003t0001g0369a0001c0003t0001g0370others(5): Show | 8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-14888T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915528 | ||||||
chr3:130915563
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(3): Show | 6 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-14853C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915563 | ||||||
chr3:130915900
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0313 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.7-14516A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130915900 | ||||||
chr3:130916005
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-14411C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916005 | ||||||
chr3:130916075
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-14341A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916075 | ||||||
chr3:130916170
|
C | T | 1 | a0001c0002t0001g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7-14246C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916170 | ||||||
chr3:130916244
|
C | CA | 34 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(31): Show | 34 | HG00609.hp2 HG01069.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-14157dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130916244 | |||||
chr3:130916370
|
C | T | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.7-14046C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916370 | ||||||
chr3:130916439
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-13977A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916439 | ||||||
chr3:130916539
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-13877A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916539 | ||||||
chr3:130916670
|
G | T | 7 | a0001c0001t0001g0337a0001c0002t0001g0215a0001c0002t0001g0338others(4): Show | 7 | HG03710.hp1 NA18946.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-13746G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916670 | ||||||
chr3:130916763
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7-13653T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916763 | ||||||
chr3:130916801
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13615A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916801 | ||||||
chr3:130916802
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13614T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916802 | ||||||
chr3:130916803
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-13613C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916803 | ||||||
chr3:130916820
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7-13596A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916820 | ||||||
chr3:130916932
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-13484A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916932 | ||||||
chr3:130916934
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-13482A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130916934 | ||||||
chr3:130917046
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.7-13370G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917046 | ||||||
chr3:130917052
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-13364C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917052 | ||||||
chr3:130917333
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-13083A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917333 | ||||||
chr3:130917503
|
A | C | 2 | a0001c0001t0002g0115a0001c0001t0012g0123 | 2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-12913A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917503 | ||||||
chr3:130917803
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.7-12613C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917803 | ||||||
chr3:130917822
|
C | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-12594C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917822 | ||||||
chr3:130917910
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-12506C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130917910 | ||||||
chr3:130917975
|
C | CT | 32 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.7-12431dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130917975 | |||||
chr3:130918000
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-12416A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918000 | ||||||
chr3:130918001
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7-12415T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918001 | ||||||
chr3:130918099
|
A | C | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.7-12317A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918099 | ||||||
chr3:130918275
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0009g0076 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7-12141A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918275 | ||||||
chr3:130918318
|
T | C | 1 | a0001c0002t0008g0327 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.7-12098T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918318 | ||||||
chr3:130918548
|
C | T | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7-11868C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918548 | ||||||
chr3:130918664
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-11752T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918664 | ||||||
chr3:130918691
|
A | C | 3 | a0001c0002t0001g0316a0001c0002t0001g0321a0001c0002t0001g0322 | 3 | HG02027.hp1 NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.7-11725A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918691 | ||||||
chr3:130918713
|
C | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-11703C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918713 | ||||||
chr3:130918720
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7-11696G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918720 | ||||||
chr3:130918724
|
G | C | 1 | a0001c0001t0001g0362 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7-11692G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918724 | ||||||
chr3:130918822
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-11594T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918822 | ||||||
chr3:130918875
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-11541C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918875 | ||||||
chr3:130918921
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-11495G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918921 | ||||||
chr3:130918980
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-11436A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918980 | ||||||
chr3:130918986
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG00639.hp1 HG01258.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-11430C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130918986 | ||||||
chr3:130919062
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-11354G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919062 | ||||||
chr3:130919230
|
C | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.7-11186C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919230 | ||||||
chr3:130919242
|
T | C | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-11174T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919242 | ||||||
chr3:130919410
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-11006G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919410 | ||||||
chr3:130919547
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7-10869A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919547 | ||||||
chr3:130919601
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-10815A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919601 | ||||||
chr3:130919655
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.7-10761C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919655 | ||||||
chr3:130919706
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.7-10710C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919706 | ||||||
chr3:130919792
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.7-10624C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919792 | ||||||
chr3:130919798
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.7-10618G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919798 | ||||||
chr3:130919804
|
C | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.7-10612C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130919804 | ||||||
chr3:130920125
|
A | T | 1 | a0001c0001t0005g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7-10291A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920125 | ||||||
chr3:130920353
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7-10063G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920353 | ||||||
chr3:130920527
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7-9889C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920527 | ||||||
chr3:130920551
|
A | G | 2 | a0001c0001t0001g0278a0001c0001t0001g0292 | 2 | NA19058.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.7-9865A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920551 | ||||||
chr3:130920645
|
G | GAT | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-9770_7-9769dupAT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130920645 | |||||
chr3:130920742
|
G | A | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-9674G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920742 | ||||||
chr3:130920814
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7-9602G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920814 | ||||||
chr3:130920969
|
A | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-9447A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130920969 | ||||||
chr3:130921024
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7-9392C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921024 | ||||||
chr3:130921079
|
C | CT | 57 | a0001c0001t0001g0002a0001c0001t0001g0056a0001c0001t0001g0064others(54): Show | 58 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.7-9317dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | |||||
chr3:130921079
|
C | CTT | 13 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0088others(10): Show | 14 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.7-9318_7-9317dupTT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | |||||
chr3:130921079
|
CT | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0173a0001c0001t0001g0257others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-9317delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130921079 | |||||
chr3:130921084
|
T | C | 49 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.7-9332T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921084 | ||||||
chr3:130921104
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0296a0001c0001t0001g0297others(1): Show | 4 | HG00140.hp1 HG02273.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-9312C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921104 | ||||||
chr3:130921168
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.7-9248G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921168 | ||||||
chr3:130921195
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.7-9221C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921195 | ||||||
chr3:130921227
|
GCC | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-9188_7-9187delCC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921227 | ||||||
chr3:130921231
|
GCCACCAC others(3): Show |
G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-9184_7-9175delCC others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921231 | ||||||
chr3:130921864
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0069 | 3 | NA18967.hp1 NA19057.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.7-8552C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921864 | ||||||
chr3:130921893
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-8523A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130921893 | ||||||
chr3:130922153
|
T | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.7-8263T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922153 | ||||||
chr3:130922361
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.7-8055C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922361 | ||||||
chr3:130922594
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-7822C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922594 | ||||||
chr3:130922867
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-7549A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922867 | ||||||
chr3:130922871
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.7-7545C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922871 | ||||||
chr3:130922872
|
G | A | 1 | a0001c0002t0001g0355 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7-7544G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130922872 | ||||||
chr3:130923001
|
A | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-7415A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923001 | ||||||
chr3:130923088
|
G | A | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.7-7328G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923088 | ||||||
chr3:130923143
|
A | G | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-7273A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923143 | ||||||
chr3:130923232
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7-7184T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923232 | ||||||
chr3:130923332
|
T | G | 2 | a0001c0003t0001g0369a0001c0003t0001g0375 | 2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.7-7084T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923332 | ||||||
chr3:130923385
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7-7031C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923385 | ||||||
chr3:130923431
|
C | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.7-6985C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923431 | ||||||
chr3:130923479
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-6937A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923479 | ||||||
chr3:130923555
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-6861A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923555 | ||||||
chr3:130923587
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-6829G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923587 | ||||||
chr3:130923686
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7-6730G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923686 | ||||||
chr3:130923833
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.7-6583C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130923833 | ||||||
chr3:130923864
|
C | CA | 33 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(30): Show | 34 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.7-6533dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130923864 | |||||
chr3:130923864
|
CA | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0088others(65): Show | 69 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.7-6533delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130923864 | |||||
chr3:130924032
|
G | A | 24 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.7-6384G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924032 | ||||||
chr3:130924147
|
GT | G | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.7-6258delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | 130924147 | |||||
chr3:130924193
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.7-6223T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924193 | ||||||
chr3:130924235
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7-6181G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924235 | ||||||
chr3:130924287
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7-6129G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924287 | ||||||
chr3:130924394
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7-6022A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924394 | ||||||
chr3:130924604
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7-5812G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924604 | ||||||
chr3:130924674
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7-5742T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924674 | ||||||
chr3:130924702
|
G | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 328 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.7-5714G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924702 | ||||||
chr3:130924768
|
T | A | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.7-5648T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924768 | ||||||
chr3:130924769
|
A | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.7-5647A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924769 | ||||||
chr3:130924852
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 108 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.7-5564C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130924852 | ||||||
chr3:130925059
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7-5357A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925059 | ||||||
chr3:130925097
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.7-5319C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925097 | ||||||
chr3:130925111
|
A | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(273): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.7-5305A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925111 | ||||||
chr3:130925215
|
A | G | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-5201A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925215 | ||||||
chr3:130925225
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-5191A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925225 | ||||||
chr3:130925428
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.7-4988G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925428 | ||||||
chr3:130925576
|
T | C | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-4840T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925576 | ||||||
chr3:130925658
|
G | A | 3 | a0001c0001t0001g0337a0001c0002t0001g0215a0001c0002t0001g0349 | 3 | NA18946.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.7-4758G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925658 | ||||||
chr3:130925735
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0169 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7-4681C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925735 | ||||||
chr3:130925831
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7-4585T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925831 | ||||||
chr3:130925938
|
A | G | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7-4478A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925938 | ||||||
chr3:130925960
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.7-4456C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925960 | ||||||
chr3:130925965
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7-4451C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130925965 | ||||||
chr3:130926001
|
T | A | 1 | a0001c0002t0001g0317 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.7-4415T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926001 | ||||||
chr3:130926085
|
T | G | 5 | a0001c0001t0001g0217a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG01081.hp1 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-4331T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926085 | ||||||
chr3:130926225
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7-4191C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926225 | ||||||
chr3:130926227
|
G | C | 4 | a0001c0001t0001g0337a0001c0002t0001g0215a0001c0002t0001g0349others(1): Show | 4 | NA18946.hp2 NA19055.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.7-4189G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926227 | ||||||
chr3:130926323
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7-4093C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926323 | ||||||
chr3:130926574
|
A | G | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-3842A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926574 | ||||||
chr3:130926618
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.7-3798A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926618 | ||||||
chr3:130926698
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.7-3718A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926698 | ||||||
chr3:130926709
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-3707C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926709 | ||||||
chr3:130926744
|
G | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.7-3672G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926744 | ||||||
chr3:130926796
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.7-3620C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926796 | ||||||
chr3:130926798
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.7-3618C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926798 | ||||||
chr3:130926844
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7-3572C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926844 | ||||||
chr3:130926882
|
A | G | 24 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.7-3534A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926882 | ||||||
chr3:130926911
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7-3505G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926911 | ||||||
chr3:130926951
|
G | A | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.7-3465G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926951 | ||||||
chr3:130926984
|
C | T | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.7-3432C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926984 | ||||||
chr3:130926988
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.7-3428C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130926988 | ||||||
chr3:130927055
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.7-3361A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927055 | ||||||
chr3:130927320
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0132 | 2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.7-3096A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927320 | ||||||
chr3:130927383
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-3033G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927383 | ||||||
chr3:130927423
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2993A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927423 | ||||||
chr3:130927465
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.7-2951T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927465 | ||||||
chr3:130927467
|
T | G | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-2949T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927467 | ||||||
chr3:130927479
|
G | A | 1 | a0002c0004t0001g0097 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7-2937G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927479 | ||||||
chr3:130927483
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7-2933C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927483 | ||||||
chr3:130927536
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7-2880C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927536 | ||||||
chr3:130927636
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.7-2780C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927636 | ||||||
chr3:130927759
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-2657A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927759 | ||||||
chr3:130927920
|
C | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2496C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130927920 | ||||||
chr3:130928086
|
C | T | 5 | a0001c0003t0001g0370a0001c0003t0001g0371a0001c0003t0001g0372others(2): Show | 5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2330C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928086 | ||||||
chr3:130928139
|
C | T | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.7-2277C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928139 | ||||||
chr3:130928467
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-1949G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928467 | ||||||
chr3:130928509
|
A | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0072 | 3 | NA18955.hp1 NA18961.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.7-1907A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928509 | ||||||
chr3:130928721
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.7-1695A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928721 | ||||||
chr3:130928752
|
A | G | 10 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(7): Show | 10 | HG02027.hp1 HG02735.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-1664A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130928752 | ||||||
chr3:130929013
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.7-1403T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929013 | ||||||
chr3:130929076
|
A | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.7-1340A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929076 | ||||||
chr3:130929383
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0165 | 3 | NA18954.hp2 NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.7-1033A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929383 | ||||||
chr3:130929386
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-1030C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929386 | ||||||
chr3:130929428
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.7-988A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929428 | ||||||
chr3:130929737
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7-679T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929737 | ||||||
chr3:130929758
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0001t0001g0127 | 3 | HG00597.hp1 NA19000.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.7-658A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929758 | ||||||
chr3:130929954
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.7-462A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130929954 | ||||||
chr3:130930010
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.7-406G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930010 | ||||||
chr3:130930020
|
A | C | 2 | a0001c0001t0002g0115a0001c0001t0012g0123 | 2 | NA18973.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.7-396A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930020 | ||||||
chr3:130930051
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.7-365G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930051 | ||||||
chr3:130930062
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.7-354G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 2/27 | chr3 | 130930062 | ||||||
chr3:130930533
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.117+7G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930533 | ||||||
chr3:130930702
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+176T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930702 | ||||||
chr3:130930795
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+269A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930795 | ||||||
chr3:130930840
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.117+314T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930840 | ||||||
chr3:130930853
|
A | G | 6 | a0001c0001t0001g0222a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+327A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930853 | ||||||
chr3:130930962
|
A | G | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.117+436A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130930962 | ||||||
chr3:130931036
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.117+510G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931036 | ||||||
chr3:130931044
|
C | A | 1 | a0001c0002t0001g0350 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.117+518C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931044 | ||||||
chr3:130931103
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+577T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931103 | ||||||
chr3:130931144
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0148 | 3 | HG03579.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.117+618T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931144 | ||||||
chr3:130931193
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+667T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931193 | ||||||
chr3:130931529
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-493A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931529 | ||||||
chr3:130931550
|
G | A | 1 | a0001c0001t0010g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-472G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931550 | ||||||
chr3:130931557
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-465C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931557 | ||||||
chr3:130931588
|
C | T | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-434C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931588 | ||||||
chr3:130931685
|
T | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0259 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.118-337T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931685 | ||||||
chr3:130931702
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.118-320T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931702 | ||||||
chr3:130931782
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-240A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931782 | ||||||
chr3:130931899
|
A | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.118-123A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 3/27 | chr3 | 130931899 | ||||||
chr3:130932156
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.234+18C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932156 | ||||||
chr3:130932216
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+78T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932216 | ||||||
chr3:130932252
|
T | C | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.234+114T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932252 | ||||||
chr3:130932396
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+258T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932396 | ||||||
chr3:130932404
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.234+266A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932404 | ||||||
chr3:130932453
|
A | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.234+315A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932453 | ||||||
chr3:130932731
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+593A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932731 | ||||||
chr3:130932929
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.234+791A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130932929 | ||||||
chr3:130933052
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.234+914G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933052 | ||||||
chr3:130933063
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+925G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933063 | ||||||
chr3:130933080
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234+942A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933080 | ||||||
chr3:130933088
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.234+950A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933088 | ||||||
chr3:130933244
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.234+1106C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933244 | ||||||
chr3:130933245
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+1107G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933245 | ||||||
chr3:130933266
|
ATTCT | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.234+1131_234+1134d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 130933266 | |||||
chr3:130933303
|
G | T | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.234+1165G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933303 | ||||||
chr3:130933491
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.235-1131A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933491 | ||||||
chr3:130933549
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.235-1073C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933549 | ||||||
chr3:130933627
|
G | T | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.235-995G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933627 | ||||||
chr3:130933679
|
G | A | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.235-943G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933679 | ||||||
chr3:130933775
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.235-847T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933775 | ||||||
chr3:130933920
|
A | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-702A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130933920 | ||||||
chr3:130934016
|
G | A | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-606G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934016 | ||||||
chr3:130934111
|
C | G | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.235-511C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934111 | ||||||
chr3:130934245
|
A | G | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-377A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934245 | ||||||
chr3:130934407
|
A | AT | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.235-205dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr3 | 130934407 | |||||
chr3:130934411
|
T | C | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.235-211T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934411 | ||||||
chr3:130934457
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.235-165G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934457 | ||||||
chr3:130934534
|
C | T | 1 | a0001c0001t0011g0283 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.235-88C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 4/27 | chr3 | 130934534 | ||||||
chr3:130934728
|
A | G | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.324+17A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130934728 | ||||||
chr3:130934918
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.324+207C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130934918 | ||||||
chr3:130935183
|
G | A | 8 | a0001c0001t0010g0112a0001c0003t0001g0369a0001c0003t0001g0370others(5): Show | 8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+472G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935183 | ||||||
chr3:130935343
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.324+632C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935343 | ||||||
chr3:130935349
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+638A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935349 | ||||||
chr3:130935474
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.324+763A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935474 | ||||||
chr3:130935479
|
A | C | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.324+768A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935479 | ||||||
chr3:130935711
|
A | G | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.324+1000A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935711 | ||||||
chr3:130935739
|
T | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.324+1028T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935739 | ||||||
chr3:130935960
|
T | G | 1 | a0001c0002t0001g0336 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.324+1249T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130935960 | ||||||
chr3:130936119
|
T | C | 4 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0336others(1): Show | 4 | HG02129.hp1 NA18997.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1309T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936119 | ||||||
chr3:130936139
|
C | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.325-1289C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936139 | ||||||
chr3:130936160
|
A | C | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-1268A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936160 | ||||||
chr3:130936213
|
T | A | 3 | a0001c0001t0001g0018a0001c0002t0001g0317a0001c0002t0001g0318 | 3 | NA18948.hp1 NA19001.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.325-1215T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936213 | ||||||
chr3:130936213
|
T | TA | 12 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0001g0144others(9): Show | 12 | HG01943.hp1 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-1205dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936213 | |||||
chr3:130936214
|
A | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG02451.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.325-1214A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936214 | ||||||
chr3:130936215
|
A | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.325-1213A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936215 | ||||||
chr3:130936231
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-1197G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936231 | ||||||
chr3:130936243
|
CCTTGGGG others(14): Show |
C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.325-1169_325-1149d others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936243 | |||||
chr3:130936260
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.325-1168G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936260 | ||||||
chr3:130936382
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG00140.hp1 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1046C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936382 | ||||||
chr3:130936383
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.325-1045G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936383 | ||||||
chr3:130936628
|
T | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.325-800T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936628 | ||||||
chr3:130936644
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325-784C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936644 | ||||||
chr3:130936773
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.325-655C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130936773 | ||||||
chr3:130936816
|
C | CA | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.325-592dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936816 | |||||
chr3:130936816
|
C | CAA | 16 | a0001c0001t0001g0191a0001c0001t0001g0209a0001c0001t0001g0211others(13): Show | 16 | HG00621.hp2 HG01175.hp2 HG03710.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-593_325-592dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130936816 | |||||
chr3:130937018
|
AT | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.325-403delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr3 | 130937018 | |||||
chr3:130937135
|
A | G | 1 | a0001c0002t0001g0339 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.325-293A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130937135 | ||||||
chr3:130937144
|
A | G | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-284A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 5/27 | chr3 | 130937144 | ||||||
chr3:130937485
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.360+22C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937485 | ||||||
chr3:130937682
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.360+219C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937682 | ||||||
chr3:130937868
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.360+405A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937868 | ||||||
chr3:130937873
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.360+410A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130937873 | ||||||
chr3:130938101
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.360+638C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938101 | ||||||
chr3:130938289
|
A | G | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.360+826A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938289 | ||||||
chr3:130938350
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.360+887A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938350 | ||||||
chr3:130938379
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+916C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938379 | ||||||
chr3:130938632
|
C | T | 27 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0116others(24): Show | 27 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.360+1169C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938632 | ||||||
chr3:130938681
|
G | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 307 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.360+1218G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938681 | ||||||
chr3:130938687
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.360+1224C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938687 | ||||||
chr3:130938808
|
A | G | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.360+1345A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130938808 | ||||||
chr3:130939245
|
C | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0265 | 2 | NA19002.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.361-1385C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939245 | ||||||
chr3:130939375
|
T | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0028others(14): Show | 19 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.361-1255T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939375 | ||||||
chr3:130939606
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.361-1024A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939606 | ||||||
chr3:130939621
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.361-1009C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939621 | ||||||
chr3:130939640
|
G | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-990G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939640 | ||||||
chr3:130939701
|
A | G | 1 | a0005c0008t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.361-929A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939701 | ||||||
chr3:130939752
|
T | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323 | 3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.361-878T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130939752 | ||||||
chr3:130940002
|
G | T | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.361-628G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130940002 | ||||||
chr3:130940486
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-144G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 6/27 | chr3 | 130940486 | ||||||
chr3:130940773
|
C | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+82C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940773 | ||||||
chr3:130940806
|
A | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG00280.hp1 HG00733.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+115A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940806 | ||||||
chr3:130940866
|
T | G | 1 | a0001c0002t0001g0351 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.422+175T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940866 | ||||||
chr3:130940873
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.422+182C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940873 | ||||||
chr3:130940905
|
A | AT | 60 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 61 | HG00438.hp1 HG00738.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.422+242dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
A | ATT | 58 | a0001c0001t0001g0016a0001c0001t0001g0094a0001c0001t0001g0106others(55): Show | 58 | HG00544.hp2 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.422+241_422+242dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
A | ATTT | 24 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0127others(21): Show | 24 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.422+240_422+242dup others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
A | ATTTT | 26 | a0001c0001t0001g0095a0001c0001t0001g0145a0001c0001t0001g0147others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.422+239_422+242dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
A | ATTTTT | 13 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(10): Show | 13 | HG01069.hp2 HG01255.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.422+238_422+242dup others(5): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
A | ATTTTTT | 7 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092others(4): Show | 7 | HG00639.hp1 HG01516.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.422+237_422+242dup others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
AT | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.422+242delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940905
|
ATTTTTTT others(6): Show |
A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+230_422+242del others(13): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940905 | |||||
chr3:130940933
|
T | A | 24 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(21): Show | 24 | HG00408.hp2 HG00609.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.422+242T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940933 | ||||||
chr3:130940933
|
T | TA | 4 | a0001c0001t0001g0275a0001c0001t0001g0295a0001c0001t0001g0299others(1): Show | 4 | HG04115.hp2 NA18950.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+243dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130940933 | |||||
chr3:130940937
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+246T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940937 | ||||||
chr3:130940938
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+247G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940938 | ||||||
chr3:130940970
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.422+279A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130940970 | ||||||
chr3:130941032
|
A | AG | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.422+342dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941032 | |||||
chr3:130941147
|
C | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.423-444C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941147 | ||||||
chr3:130941147
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.423-444C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941147 | ||||||
chr3:130941163
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-428C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941163 | ||||||
chr3:130941222
|
C | CTGTGTGT others(1): Show |
5 | a0001c0003t0001g0369a0001c0003t0001g0370a0001c0003t0001g0371others(2): Show | 5 | HG00733.hp1 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-369_423-368ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | ||||||
chr3:130941222
|
C | CTGTGTGT others(3): Show |
1 | a0001c0003t0001g0373 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423-369_423-368ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | ||||||
chr3:130941222
|
CAGTG | C | 4 | a0001c0001t0001g0102a0001c0001t0001g0313a0003c0005t0003g0100others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-368_423-365del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941222 | ||||||
chr3:130941223
|
A | AGT | 24 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0044others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.423-327_423-326dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
A | AGTGT | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-329_423-326dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423-335_423-326dup others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
A | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(13): Show | 17 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.423-368A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941223 | ||||||
chr3:130941223
|
AGT | A | 18 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0059others(15): Show | 18 | HG00741.hp2 HG01884.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-327_423-326del others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGT | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0041others(5): Show | 8 | HG00597.hp1 HG01167.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.423-329_423-326del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGT | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0080others(16): Show | 19 | HG02027.hp1 HG02293.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.423-331_423-326del others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGTG others(1): Show |
A | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.423-333_423-326del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGTG others(3): Show |
A | 47 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0093others(44): Show | 47 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.423-335_423-326del others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0175a0001c0001t0001g0340 | 2 | NA18990.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.423-337_423-326del others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGTG others(7): Show |
A | 10 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(7): Show | 11 | HG01243.hp2 HG02280.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-339_423-326del others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941223
|
AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.423-343_423-326del others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941223 | |||||
chr3:130941252
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.423-339G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941252 | ||||||
chr3:130941252
|
G | GTGTGTC | 4 | a0001c0001t0001g0146a0001c0001t0001g0363a0001c0001t0001g0365others(1): Show | 4 | HG01099.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-334_423-333ins others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941252
|
G | GTGTGTCT others(23): Show |
4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(1): Show | 4 | HG01255.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-334_423-333ins others(30): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941252
|
G | GTGTGTGT others(1): Show |
32 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0143others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.423-332_423-331ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941252
|
G | GTGTGTGT others(3): Show |
5 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG00639.hp1 HG01258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.423-330_423-329ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941252
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0314 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.423-328_423-315dup others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941252
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.423-326_423-325ins others(18): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941252 | |||||
chr3:130941254
|
G | GTGTGTGT others(1): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.423-330_423-329ins others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941254 | |||||
chr3:130941254
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0017 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.423-328_423-327ins others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941254 | |||||
chr3:130941266
|
C | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0135a0001c0001t0001g0167others(1): Show | 4 | HG02486.hp2 NA18969.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-325C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941266 | ||||||
chr3:130941268
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.423-323G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941268 | ||||||
chr3:130941275
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 10 | HG01243.hp2 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.423-316T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941275 | ||||||
chr3:130941283
|
C | CA | 3 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0087 | 3 | HG02818.hp2 NA18940.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.423-308_423-307ins others(1): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941283 | ||||||
chr3:130941283
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.423-308C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941283 | ||||||
chr3:130941283
|
CGCGCGCA others(1): Show |
C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-305_423-298del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr3 | 130941283 | |||||
chr3:130941327
|
C | A | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.423-264C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941327 | ||||||
chr3:130941431
|
T | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-160T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 7/27 | chr3 | 130941431 | ||||||
chr3:130941709
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.531+10G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941709 | ||||||
chr3:130941777
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.531+78A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941777 | ||||||
chr3:130941964
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+265C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130941964 | ||||||
chr3:130942041
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.531+342G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942041 | ||||||
chr3:130942139
|
A | G | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.531+440A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942139 | ||||||
chr3:130942145
|
A | C | 1 | a0001c0002t0001g0335 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.531+446A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942145 | ||||||
chr3:130942164
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.531+465A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942164 | ||||||
chr3:130942259
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.531+560G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942259 | ||||||
chr3:130942393
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+694T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942393 | ||||||
chr3:130942448
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0028others(15): Show | 20 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.531+749C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942448 | ||||||
chr3:130942455
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+756G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942455 | ||||||
chr3:130942456
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+757T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942456 | ||||||
chr3:130942471
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.531+772C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942471 | ||||||
chr3:130942528
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.531+829A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942528 | ||||||
chr3:130942564
|
G | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG01069.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+865G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942564 | ||||||
chr3:130942567
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.531+868G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942567 | ||||||
chr3:130942758
|
T | G | 1 | a0001c0001t0001g0311 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.531+1059T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130942758 | ||||||
chr3:130943123
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.531+1424C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943123 | ||||||
chr3:130943164
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.531+1465G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943164 | ||||||
chr3:130943307
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.531+1608C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943307 | ||||||
chr3:130943506
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.531+1807C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943506 | ||||||
chr3:130943658
|
T | C | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | NA18946.hp1 NA18964.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+1959T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130943658 | ||||||
chr3:130944104
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.531+2405G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944104 | ||||||
chr3:130944145
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.531+2446C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944145 | ||||||
chr3:130944410
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+2711A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944410 | ||||||
chr3:130944611
|
G | T | 3 | a0002c0004t0001g0097a0002c0004t0001g0098a0002c0004t0001g0099 | 3 | HG02630.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.531+2912G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944611 | ||||||
chr3:130944784
|
A | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.531+3085A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944784 | ||||||
chr3:130944938
|
T | C | 1 | a0001c0002t0001g0355 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.531+3239T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130944938 | ||||||
chr3:130945453
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+3754G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945453 | ||||||
chr3:130945487
|
TA | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 315 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.531+3790delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130945487 | |||||
chr3:130945524
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+3825C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945524 | ||||||
chr3:130945757
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.531+4058G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945757 | ||||||
chr3:130945901
|
G | GT | 6 | a0001c0001t0001g0113a0001c0001t0001g0131a0001c0001t0001g0167others(3): Show | 6 | HG01109.hp1 HG02027.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+4217dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130945901 | |||||
chr3:130945995
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+4296T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130945995 | ||||||
chr3:130946043
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.531+4344T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946043 | ||||||
chr3:130946255
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+4556C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946255 | ||||||
chr3:130946502
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+4803C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946502 | ||||||
chr3:130946560
|
C | T | 4 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0336others(1): Show | 4 | HG02129.hp1 NA18997.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+4861C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946560 | ||||||
chr3:130946564
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.531+4865C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946564 | ||||||
chr3:130946687
|
A | G | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+4988A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946687 | ||||||
chr3:130946964
|
A | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.531+5265A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946964 | ||||||
chr3:130946979
|
C | T | 50 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.531+5280C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130946979 | ||||||
chr3:130947015
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.531+5316T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947015 | ||||||
chr3:130947017
|
A | G | 2 | a0001c0001t0001g0194a0005c0008t0001g0193 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.531+5318A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947017 | ||||||
chr3:130947060
|
C | G | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.531+5361C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947060 | ||||||
chr3:130947065
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.531+5366C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947065 | ||||||
chr3:130947251
|
TA | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+5563delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130947251 | |||||
chr3:130947263
|
T | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0237a0001c0001t0001g0249others(1): Show | 4 | HG01891.hp2 HG01981.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+5564T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947263 | ||||||
chr3:130947329
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01358.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531+5630T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947329 | ||||||
chr3:130947330
|
T | A | 1 | a0001c0002t0001g0343 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.531+5631T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947330 | ||||||
chr3:130947527
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0134 | 2 | HG04184.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.531+5828A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947527 | ||||||
chr3:130947893
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.532-5928T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130947893 | ||||||
chr3:130948166
|
T | A | 2 | a0001c0002t0001g0321a0001c0002t0001g0322 | 2 | NA18945.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.532-5655T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948166 | ||||||
chr3:130948269
|
TGTTTA | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-5551_532-5547d others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948269 | ||||||
chr3:130948328
|
G | A | 1 | a0001c0001t0012g0123 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.532-5493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948328 | ||||||
chr3:130948346
|
G | GT | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-5465dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130948346 | |||||
chr3:130948346
|
GT | G | 8 | a0001c0001t0010g0112a0001c0003t0001g0369a0001c0003t0001g0370others(5): Show | 8 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.532-5465delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130948346 | |||||
chr3:130948436
|
TG | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-5384delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948436 | ||||||
chr3:130948444
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.532-5377G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948444 | ||||||
chr3:130948583
|
T | C | 1 | a0001c0003t0001g0374 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.532-5238T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948583 | ||||||
chr3:130948635
|
C | T | 5 | a0001c0002t0001g0324a0001c0002t0001g0333a0001c0002t0001g0343others(2): Show | 5 | HG00597.hp2 NA18968.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-5186C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948635 | ||||||
chr3:130948691
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.532-5130A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948691 | ||||||
chr3:130948964
|
T | C | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-4857T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130948964 | ||||||
chr3:130949155
|
T | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.532-4666T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949155 | ||||||
chr3:130949273
|
A | T | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.532-4548A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949273 | ||||||
chr3:130949324
|
C | T | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-4497C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949324 | ||||||
chr3:130949403
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-4418G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949403 | ||||||
chr3:130949409
|
G | A | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.532-4412G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949409 | ||||||
chr3:130949637
|
AC | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-4183delC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949637 | ||||||
chr3:130949667
|
C | T | 12 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.532-4154C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949667 | ||||||
chr3:130949763
|
TAGTA | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.532-4054_532-4051d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130949763 | |||||
chr3:130949910
|
G | A | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.532-3911G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949910 | ||||||
chr3:130949986
|
T | C | 5 | a0001c0001t0001g0217a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG01081.hp1 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-3835T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130949986 | ||||||
chr3:130950036
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0007g0178 | 2 | HG00558.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.532-3785C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950036 | ||||||
chr3:130950247
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-3574T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950247 | ||||||
chr3:130950429
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.532-3392G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950429 | ||||||
chr3:130950551
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.532-3270T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130950551 | ||||||
chr3:130950876
|
T | TA | 19 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(16): Show | 20 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.532-2934dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | |||||
chr3:130950876
|
T | TAA | 7 | a0001c0003t0001g0369a0001c0003t0001g0370a0001c0003t0001g0371others(4): Show | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-2935_532-2934d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | |||||
chr3:130950876
|
TA | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.532-2934delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130950876 | |||||
chr3:130951263
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.532-2558A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951263 | ||||||
chr3:130951327
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-2494C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951327 | ||||||
chr3:130951367
|
A | C | 2 | a0001c0002t0001g0338a0001c0002t0001g0339 | 2 | NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.532-2454A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951367 | ||||||
chr3:130951521
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.532-2300C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951521 | ||||||
chr3:130951625
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-2196T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951625 | ||||||
chr3:130951655
|
G | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0072 | 3 | NA18955.hp1 NA18961.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.532-2166G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951655 | ||||||
chr3:130951827
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0313 | 2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.532-1994A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951827 | ||||||
chr3:130951961
|
T | TTA | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-1858_532-1857d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130951961 | |||||
chr3:130951971
|
C | T | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.532-1850C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130951971 | ||||||
chr3:130952173
|
T | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 328 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.532-1648T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952173 | ||||||
chr3:130952195
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.532-1626A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952195 | ||||||
chr3:130952318
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.532-1503A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952318 | ||||||
chr3:130952447
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.532-1374G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952447 | ||||||
chr3:130952468
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.532-1353T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952468 | ||||||
chr3:130952524
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-1297T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952524 | ||||||
chr3:130952845
|
C | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(8): Show | 12 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.532-976C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952845 | ||||||
chr3:130952896
|
A | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.532-925A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130952896 | ||||||
chr3:130953076
|
C | CGTAT | 54 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(51): Show | 54 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.532-708_532-705dup others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953076
|
C | CGTATGTA others(1): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0145a0001c0001t0001g0148 | 3 | HG02723.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.532-712_532-705dup others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953076
|
C | CGTATGTA others(5): Show |
1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.532-716_532-705dup others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953076
|
C | CGTATGTA others(9): Show |
1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.532-720_532-705dup others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953076
|
CGTAT | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.532-708_532-705del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953076
|
CGTATGTA others(1): Show |
C | 40 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0081others(37): Show | 41 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.532-712_532-705del others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953076 | |||||
chr3:130953436
|
GT | G | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(12): Show | 15 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.532-381delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr3 | 130953436 | |||||
chr3:130953456
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.532-365A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953456 | ||||||
chr3:130953557
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.532-264T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953557 | ||||||
chr3:130953678
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.532-143T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 8/27 | chr3 | 130953678 | ||||||
chr3:130954158
|
G | A | 1 | a0001c0002t0001g0318 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.687+182G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954158 | ||||||
chr3:130954331
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0009g0076 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.687+355G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954331 | ||||||
chr3:130954414
|
C | T | 2 | a0001c0002t0001g0342a0001c0002t0001g0354 | 2 | HG01081.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.687+438C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954414 | ||||||
chr3:130954469
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0260 | 3 | HG00280.hp1 NA20300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.687+493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954469 | ||||||
chr3:130954525
|
G | A | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.688-487G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954525 | ||||||
chr3:130954681
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092 | 3 | HG00639.hp1 HG01516.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.688-331T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954681 | ||||||
chr3:130954733
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.688-279C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954733 | ||||||
chr3:130954765
|
G | A | 1 | a0001c0001t0001g0367 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.688-247G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954765 | ||||||
chr3:130954861
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.688-151A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954861 | ||||||
chr3:130954898
|
T | C | 2 | a0001c0003t0001g0371a0001c0003t0001g0372 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.688-114T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 9/27 | chr3 | 130954898 | ||||||
chr3:130955139
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.756+59G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955139 | ||||||
chr3:130955178
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.756+98A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955178 | ||||||
chr3:130955221
|
A | G | 2 | a0001c0001t0001g0166a0001c0002t0001g0344 | 2 | HG02735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.756+141A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955221 | ||||||
chr3:130955227
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.756+147G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955227 | ||||||
chr3:130955240
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.756+160T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955240 | ||||||
chr3:130955346
|
T | C | 1 | a0001c0002t0001g0350 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.756+266T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955346 | ||||||
chr3:130955633
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-471G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955633 | ||||||
chr3:130955634
|
A | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA19067.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.757-470A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955634 | ||||||
chr3:130955734
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.757-370A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 10/27 | chr3 | 130955734 | ||||||
chr3:130956444
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.832+265T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956444 | ||||||
chr3:130956504
|
A | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131 | 3 | NA18988.hp1 NA18991.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.832+325A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956504 | ||||||
chr3:130956532
|
G | T | 1 | a0001c0002t0001g0322 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.832+353G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956532 | ||||||
chr3:130956610
|
G | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.832+431G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956610 | ||||||
chr3:130956622
|
A | C | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+443A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956622 | ||||||
chr3:130956912
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.832+733G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956912 | ||||||
chr3:130956943
|
A | G | 15 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(12): Show | 16 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.832+764A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130956943 | ||||||
chr3:130957006
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.832+827T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957006 | ||||||
chr3:130957424
|
T | C | 1 | a0001c0001t0001g0359 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.832+1245T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957424 | ||||||
chr3:130957460
|
G | A | 49 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.832+1281G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957460 | ||||||
chr3:130957477
|
G | A | 32 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+1298G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957477 | ||||||
chr3:130957478
|
G | A | 32 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(29): Show | 32 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+1299G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957478 | ||||||
chr3:130957836
|
T | C | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-1439T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957836 | ||||||
chr3:130957848
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.833-1427G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957848 | ||||||
chr3:130957868
|
A | G | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-1407A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130957868 | ||||||
chr3:130958041
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.833-1234T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958041 | ||||||
chr3:130958052
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-1223G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958052 | ||||||
chr3:130958069
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.833-1206A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958069 | ||||||
chr3:130958174
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.833-1101A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958174 | ||||||
chr3:130958280
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.833-995G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958280 | ||||||
chr3:130958329
|
A | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | NA18948.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.833-946A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958329 | ||||||
chr3:130958478
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.833-797C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958478 | ||||||
chr3:130958486
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.833-789G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958486 | ||||||
chr3:130958701
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.833-574T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958701 | ||||||
chr3:130958766
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.833-509C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958766 | ||||||
chr3:130958870
|
A | G | 45 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(42): Show | 45 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.833-405A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958870 | ||||||
chr3:130958964
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.833-311A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130958964 | ||||||
chr3:130959193
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.833-82G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130959193 | ||||||
chr3:130959209
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.833-66G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 11/27 | chr3 | 130959209 | ||||||
chr3:130959419
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.899+78T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959419 | ||||||
chr3:130959584
|
A | T | 23 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.899+243A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959584 | ||||||
chr3:130959585
|
T | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.899+244T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959585 | ||||||
chr3:130959626
|
C | A | 6 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 6 | HG00738.hp1 HG02300.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+285C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959626 | ||||||
chr3:130959751
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.899+410A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130959751 | ||||||
chr3:130960040
|
A | T | 1 | a0001c0002t0001g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.899+699A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960040 | ||||||
chr3:130960326
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.899+985C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960326 | ||||||
chr3:130960343
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.899+1002A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960343 | ||||||
chr3:130960480
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+1139T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960480 | ||||||
chr3:130960634
|
C | G | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.899+1293C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960634 | ||||||
chr3:130960638
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.899+1297T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960638 | ||||||
chr3:130960641
|
A | C | 1 | a0001c0002t0001g0332 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.899+1300A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960641 | ||||||
chr3:130960733
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.899+1392A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130960733 | ||||||
chr3:130961116
|
A | C | 1 | a0001c0001t0001g0245 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.899+1775A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961116 | ||||||
chr3:130961198
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0024 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.899+1857T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961198 | ||||||
chr3:130961250
|
GT | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 147 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.899+1922delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961250 | |||||
chr3:130961250
|
GTT | G | 157 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(154): Show | 157 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.899+1921_899+1922d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961250 | |||||
chr3:130961780
|
T | C | 81 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0275others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.900-2191T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961780 | ||||||
chr3:130961785
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 59 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.900-2186A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961785 | ||||||
chr3:130961853
|
A | AG | 5 | a0001c0003t0001g0370a0001c0003t0001g0371a0001c0003t0001g0372others(2): Show | 5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.900-2116dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130961853 | |||||
chr3:130961943
|
C | A | 1 | a0001c0001t0001g0312 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.900-2028C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961943 | ||||||
chr3:130961968
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.900-2003G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130961968 | ||||||
chr3:130962302
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.900-1669A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962302 | ||||||
chr3:130962398
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900-1573T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962398 | ||||||
chr3:130962478
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.900-1493G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962478 | ||||||
chr3:130962492
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1479G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962492 | ||||||
chr3:130962551
|
T | C | 30 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.900-1420T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962551 | ||||||
chr3:130962715
|
TA | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.900-1239delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130962715 | |||||
chr3:130962715
|
TAA | T | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.900-1240_900-1239d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr3 | 130962715 | |||||
chr3:130962738
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 6 | HG02818.hp2 HG02895.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.900-1233G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962738 | ||||||
chr3:130962807
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.900-1164A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962807 | ||||||
chr3:130962849
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.900-1122A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130962849 | ||||||
chr3:130963043
|
T | C | 1 | a0001c0003t0001g0369 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.900-928T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963043 | ||||||
chr3:130963216
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.900-755G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963216 | ||||||
chr3:130963239
|
G | A | 81 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0275others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.900-732G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963239 | ||||||
chr3:130963382
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.900-589T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963382 | ||||||
chr3:130963818
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0170 | 2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.900-153A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 12/27 | chr3 | 130963818 | ||||||
chr3:130964132
|
C | T | 34 | a0001c0001t0001g0077a0001c0001t0001g0275a0001c0001t0001g0276others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1024+37C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964132 | ||||||
chr3:130964161
|
C | CA | 46 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323others(43): Show | 46 | HG00597.hp2 HG00735.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1024+67dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr3 | 130964161 | |||||
chr3:130964217
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 10 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024+122A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964217 | ||||||
chr3:130964366
|
A | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1024+271A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964366 | ||||||
chr3:130964373
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1024+278A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964373 | ||||||
chr3:130964508
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+413A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964508 | ||||||
chr3:130964662
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025-286G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964662 | ||||||
chr3:130964840
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-108A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964840 | ||||||
chr3:130964901
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-47A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 13/27 | chr3 | 130964901 | ||||||
chr3:130965165
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1122+120T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965165 | ||||||
chr3:130965194
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+149C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965194 | ||||||
chr3:130965225
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1122+180A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965225 | ||||||
chr3:130965504
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1122+459G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965504 | ||||||
chr3:130965574
|
C | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1122+529C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965574 | ||||||
chr3:130965580
|
C | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 317 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1122+535C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965580 | ||||||
chr3:130965769
|
G | A | 81 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0275others(78): Show | 81 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1122+724G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965769 | ||||||
chr3:130965779
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1122+734G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130965779 | ||||||
chr3:130966142
|
CA | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1123-1002delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966142 | ||||||
chr3:130966425
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-720T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966425 | ||||||
chr3:130966560
|
A | C | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1123-585A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966560 | ||||||
chr3:130966562
|
T | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1123-583T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966562 | ||||||
chr3:130966803
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-342C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966803 | ||||||
chr3:130966850
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1123-295A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966850 | ||||||
chr3:130966913
|
T | C | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1123-232T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966913 | ||||||
chr3:130966946
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-199G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966946 | ||||||
chr3:130966965
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-180A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130966965 | ||||||
chr3:130967002
|
A | T | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1123-143A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | chr3 | 130967002 | ||||||
chr3:130967022
|
CT | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1123-119delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr3 | 130967022 | |||||
chr3:130967571
|
T | C | 4 | a0001c0001t0001g0337a0001c0002t0001g0215a0001c0002t0001g0349others(1): Show | 4 | NA18946.hp2 NA19055.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+152T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967571 | ||||||
chr3:130967571
|
T | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308+152T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967571 | ||||||
chr3:130967821
|
CTT | C | 5 | a0001c0003t0001g0370a0001c0003t0001g0371a0001c0003t0001g0372others(2): Show | 5 | HG02258.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1308+404_1308+405d others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr3 | 130967821 | |||||
chr3:130967847
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1308+428C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967847 | ||||||
chr3:130967870
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1308+451G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967870 | ||||||
chr3:130967933
|
T | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0068 | 2 | HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1308+514T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130967933 | ||||||
chr3:130968073
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1308+654C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968073 | ||||||
chr3:130968250
|
G | A | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1308+831G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968250 | ||||||
chr3:130968338
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1308+919A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968338 | ||||||
chr3:130968388
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG02027.hp2 NA18747.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309-904C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968388 | ||||||
chr3:130968627
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1309-665A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968627 | ||||||
chr3:130968718
|
T | G | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1309-574T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968718 | ||||||
chr3:130968805
|
C | G | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1309-487C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968805 | ||||||
chr3:130968860
|
C | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 317 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1309-432C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130968860 | ||||||
chr3:130969113
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309-179T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 16/27 | chr3 | 130969113 | ||||||
chr3:130969472
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1413+76G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130969472 | ||||||
chr3:130969585
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+189A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130969585 | ||||||
chr3:130970036
|
G | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1413+640G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970036 | ||||||
chr3:130970050
|
G | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+654G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970050 | ||||||
chr3:130970055
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1413+659C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970055 | ||||||
chr3:130970089
|
G | A | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1413+693G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970089 | ||||||
chr3:130970183
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1413+787T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970183 | ||||||
chr3:130970369
|
T | TAC | 60 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(57): Show | 61 | HG00639.hp2 HG00741.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.1413+1010_1413+101 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACAC | 56 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0088others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1413+1008_1413+101 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACAC | 90 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0080others(87): Show | 91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1413+1006_1413+101 others(10): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(1): Show |
39 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0105others(36): Show | 40 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1413+1004_1413+101 others(12): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(3): Show |
17 | a0001c0001t0001g0108a0001c0001t0001g0133a0001c0001t0001g0211others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1413+1002_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0210others(5): Show | 8 | HG01123.hp2 HG02809.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1413+1000_1413+101 others(16): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1413+998_1413+1011 others(17): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1413+996_1413+1011 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+994_1413+1011 others(21): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
TAC | T | 17 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 17 | HG01943.hp2 HG02040.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1413+1010_1413+101 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
TACAC | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0077 | 5 | NA18941.hp1 NA18944.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413+1008_1413+101 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
TACACACA others(3): Show |
T | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1413+1002_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+996_1413+1011 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970369
|
TACACACA others(13): Show |
T | 1 | a0001c0002t0001g0335 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1413+992_1413+1011 others(23): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970369 | |||||
chr3:130970406
|
A | ACACACAC others(3): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130970406 | |||||
chr3:130970407
|
C | CACACA | 3 | a0001c0001t0001g0127a0001c0001t0001g0243a0001c0001t0001g0366 | 3 | HG01175.hp2 HG03927.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(9): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | ||||||
chr3:130970407
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C | CACACACA | 3 | a0001c0001t0001g0131a0001c0001t0001g0247a0001c0001t0001g0265 | 3 | NA18991.hp1 NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1413+1011_1413+101 others(11): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | ||||||
chr3:130970407
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1413+1011_1413+101 others(15): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970407 | ||||||
chr3:130970479
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C | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | HG01069.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+1083C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970479 | ||||||
chr3:130970490
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+1094A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970490 | ||||||
chr3:130970632
|
G | T | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1413+1236G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970632 | ||||||
chr3:130970812
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G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+1416G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970812 | ||||||
chr3:130970845
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1413+1449G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970845 | ||||||
chr3:130970918
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A | G | 35 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0275others(32): Show | 35 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1413+1522A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130970918 | ||||||
chr3:130971147
|
G | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092 | 3 | HG00639.hp1 HG01516.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1413+1751G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971147 | ||||||
chr3:130971220
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413+1824T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971220 | ||||||
chr3:130971230
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA19067.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1413+1834C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971230 | ||||||
chr3:130971544
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1413+2148T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971544 | ||||||
chr3:130971729
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1413+2333C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971729 | ||||||
chr3:130971769
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1413+2373T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971769 | ||||||
chr3:130971890
|
C | G | 1 | a0001c0002t0001g0350 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1413+2494C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971890 | ||||||
chr3:130971950
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02723.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413+2554A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971950 | ||||||
chr3:130971991
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1413+2595C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130971991 | ||||||
chr3:130972078
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1413+2682C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972078 | ||||||
chr3:130972092
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1413+2696A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972092 | ||||||
chr3:130972098
|
A | G | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1413+2702A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972098 | ||||||
chr3:130972142
|
A | G | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1413+2746A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972142 | ||||||
chr3:130972204
|
G | A | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1413+2808G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972204 | ||||||
chr3:130972230
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1413+2834C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972230 | ||||||
chr3:130972285
|
TG | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1413+2890delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972285 | ||||||
chr3:130972348
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1413+2952C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972348 | ||||||
chr3:130972472
|
C | CT | 11 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0002t0001g0334others(8): Show | 11 | HG00597.hp1 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1414-2846dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | |||||
chr3:130972472
|
C | CTT | 9 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 10 | HG01243.hp2 HG01346.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1414-2847_1414-284 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | |||||
chr3:130972472
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1414-2860C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972472 | ||||||
chr3:130972472
|
CT | C | 45 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(42): Show | 45 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1414-2846delT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972472 | |||||
chr3:130972485
|
T | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | NA19007.hp2 NA19043.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1414-2847T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972485 | ||||||
chr3:130972487
|
A | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414-2845A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972487 | ||||||
chr3:130972525
|
C | G | 33 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1414-2807C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972525 | ||||||
chr3:130972589
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1414-2743C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972589 | ||||||
chr3:130972617
|
T | TC | 41 | a0001c0001t0001g0261a0001c0001t0001g0319a0001c0001t0001g0320others(38): Show | 41 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1414-2710dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972617 | |||||
chr3:130972623
|
T | TC | 28 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0034others(25): Show | 28 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1414-2703dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130972623 | |||||
chr3:130972628
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1414-2704C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972628 | ||||||
chr3:130972659
|
C | T | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1414-2673C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972659 | ||||||
chr3:130972710
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0156 | 2 | HG02451.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1414-2622C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972710 | ||||||
chr3:130972820
|
T | C | 5 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | NA18978.hp2 NA18989.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-2512T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130972820 | ||||||
chr3:130973004
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 85 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1414-2328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973004 | ||||||
chr3:130973069
|
T | TAAG | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 124 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1414-2261_1414-226 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr3 | 130973069 | |||||
chr3:130973245
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 122 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1414-2087T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973245 | ||||||
chr3:130973268
|
A | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0072others(1): Show | 4 | NA18955.hp1 NA18961.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-2064A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973268 | ||||||
chr3:130973341
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1414-1991C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973341 | ||||||
chr3:130973512
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1414-1820G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973512 | ||||||
chr3:130973558
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1414-1774C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973558 | ||||||
chr3:130973687
|
T | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1414-1645T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973687 | ||||||
chr3:130973772
|
A | G | 69 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1414-1560A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973772 | ||||||
chr3:130973885
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1414-1447A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973885 | ||||||
chr3:130973892
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1414-1440A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973892 | ||||||
chr3:130973966
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1414-1366G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130973966 | ||||||
chr3:130974098
|
T | C | 7 | a0001c0003t0001g0369a0001c0003t0001g0370a0001c0003t0001g0371others(4): Show | 7 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-1234T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974098 | ||||||
chr3:130974236
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1414-1096A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974236 | ||||||
chr3:130974327
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1414-1005T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974327 | ||||||
chr3:130974329
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG00639.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1414-1003G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974329 | ||||||
chr3:130974378
|
A | G | 3 | a0001c0002t0001g0215a0001c0002t0001g0349a0001c0002t0001g0350 | 3 | NA19055.hp2 NA19072.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1414-954A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974378 | ||||||
chr3:130974736
|
G | A | 1 | a0001c0001t0010g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1414-596G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974736 | ||||||
chr3:130974847
|
C | T | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 151 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1414-485C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974847 | ||||||
chr3:130974961
|
T | C | 1 | a0003c0005t0003g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1414-371T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974961 | ||||||
chr3:130974983
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414-349A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974983 | ||||||
chr3:130974992
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1414-340G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130974992 | ||||||
chr3:130975259
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1414-73C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130975259 | ||||||
chr3:130975266
|
T | C | 6 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 6 | HG00544.hp2 HG00621.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414-66T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 17/27 | chr3 | 130975266 | ||||||
chr3:130975510
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1570+22C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975510 | ||||||
chr3:130975662
|
A | G | 16 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(13): Show | 16 | HG00609.hp2 HG02074.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1570+174A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975662 | ||||||
chr3:130975709
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1570+221A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130975709 | ||||||
chr3:130976179
|
A | C | 1 | a0002c0004t0001g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1570+691A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976179 | ||||||
chr3:130976334
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+846T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976334 | ||||||
chr3:130976418
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1570+930C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976418 | ||||||
chr3:130976480
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1570+992T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976480 | ||||||
chr3:130976501
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0236 | 2 | HG02129.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1570+1013C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976501 | ||||||
chr3:130976715
|
T | C | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1570+1227T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976715 | ||||||
chr3:130976755
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1570+1267C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976755 | ||||||
chr3:130976755
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1570+1267C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976755 | ||||||
chr3:130976882
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1570+1394C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976882 | ||||||
chr3:130976919
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+1431A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976919 | ||||||
chr3:130976984
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1570+1496C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130976984 | ||||||
chr3:130977006
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1570+1518C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977006 | ||||||
chr3:130977118
|
T | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1570+1630T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977118 | ||||||
chr3:130977146
|
A | G | 1 | a0001c0001t0010g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1570+1658A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977146 | ||||||
chr3:130977172
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1570+1684C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977172 | ||||||
chr3:130977186
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0259 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1570+1698G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977186 | ||||||
chr3:130977318
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1570+1830A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977318 | ||||||
chr3:130977328
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+1840T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977328 | ||||||
chr3:130977468
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1571-1781C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977468 | ||||||
chr3:130977539
|
G | A | 24 | a0001c0002t0001g0215a0001c0002t0001g0315a0001c0002t0001g0324others(21): Show | 24 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1571-1710G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977539 | ||||||
chr3:130977665
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1571-1584A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977665 | ||||||
chr3:130977669
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1571-1580T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977669 | ||||||
chr3:130977774
|
A | G | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1571-1475A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977774 | ||||||
chr3:130977885
|
T | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1571-1364T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977885 | ||||||
chr3:130977980
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1571-1269A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130977980 | ||||||
chr3:130978122
|
G | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1127G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978122 | ||||||
chr3:130978124
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1125C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978124 | ||||||
chr3:130978125
|
C | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1571-1124C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978125 | ||||||
chr3:130978130
|
C | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02273.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1571-1119C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978130 | ||||||
chr3:130978141
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02615.hp1 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571-1108A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978141 | ||||||
chr3:130978188
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1571-1061G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978188 | ||||||
chr3:130978358
|
T | G | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1571-891T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978358 | ||||||
chr3:130978466
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1571-783C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978466 | ||||||
chr3:130978474
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1571-775C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978474 | ||||||
chr3:130978594
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1571-655T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978594 | ||||||
chr3:130978920
|
T | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1571-329T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978920 | ||||||
chr3:130978955
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1571-294T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130978955 | ||||||
chr3:130979082
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1571-167T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979082 | ||||||
chr3:130979172
|
A | G | 1 | a0001c0002t0001g0354 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1571-77A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979172 | ||||||
chr3:130979178
|
T | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0237a0001c0001t0001g0249others(1): Show | 4 | HG01891.hp2 HG01981.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-71T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 18/27 | chr3 | 130979178 | ||||||
chr3:130979450
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1741+31A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979450 | ||||||
chr3:130979468
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0127 | 2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1741+49C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979468 | ||||||
chr3:130979471
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1741+52T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979471 | ||||||
chr3:130979541
|
G | A | 1 | a0001c0002t0001g0343 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1741+122G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979541 | ||||||
chr3:130979674
|
TC | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 102 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1741+256delC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130979674 | ||||||
chr3:130979683
|
CA | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1741+266delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr3 | 130979683 | |||||
chr3:130980070
|
C | T | 1 | a0005c0008t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1742-512C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980070 | ||||||
chr3:130980254
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1742-328T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980254 | ||||||
chr3:130980256
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1742-326T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980256 | ||||||
chr3:130980282
|
T | TG | 7 | a0001c0001t0001g0222a0001c0001t0001g0245a0001c0001t0001g0301others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742-299dupG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr3 | 130980282 | |||||
chr3:130980313
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1742-269T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980313 | ||||||
chr3:130980345
|
A | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01255.hp1 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1742-237A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 19/27 | chr3 | 130980345 | ||||||
chr3:130980942
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1839+263A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130980942 | ||||||
chr3:130980973
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323 | 3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1839+294A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130980973 | ||||||
chr3:130981111
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1839+432A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981111 | ||||||
chr3:130981145
|
G | A | 1 | a0001c0002t0001g0335 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1839+466G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981145 | ||||||
chr3:130981183
|
G | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1839+504G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981183 | ||||||
chr3:130981272
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1839+593T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981272 | ||||||
chr3:130981291
|
T | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+612T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981291 | ||||||
chr3:130981381
|
T | C | 3 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0311 | 3 | HG02155.hp1 HG02523.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1839+702T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981381 | ||||||
chr3:130981428
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1839+749A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981428 | ||||||
chr3:130981814
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+1135T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981814 | ||||||
chr3:130981894
|
A | G | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1839+1215A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130981894 | ||||||
chr3:130982097
|
C | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1418C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982097 | ||||||
chr3:130982119
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1839+1440G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982119 | ||||||
chr3:130982214
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+1535G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982214 | ||||||
chr3:130982338
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1839+1659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982338 | ||||||
chr3:130982346
|
G | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+1667G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982346 | ||||||
chr3:130982367
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+1688A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982367 | ||||||
chr3:130982420
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1839+1741C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982420 | ||||||
chr3:130982421
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1839+1742T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982421 | ||||||
chr3:130982450
|
G | T | 1 | a0001c0006t0001g0263 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1839+1771G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982450 | ||||||
chr3:130982467
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0009g0076 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1839+1788C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982467 | ||||||
chr3:130982474
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+1795C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982474 | ||||||
chr3:130982524
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1839+1845C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982524 | ||||||
chr3:130982581
|
T | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1902T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982581 | ||||||
chr3:130982706
|
A | G | 46 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1839+2027A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982706 | ||||||
chr3:130982757
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1839+2078A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982757 | ||||||
chr3:130982763
|
T | C | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1839+2084T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982763 | ||||||
chr3:130982836
|
G | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+2157G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982836 | ||||||
chr3:130982967
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(18): Show | 22 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1839+2288T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130982967 | ||||||
chr3:130983105
|
T | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+2426T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983105 | ||||||
chr3:130983107
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 122 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1839+2428T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983107 | ||||||
chr3:130983109
|
G | T | 8 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 8 | HG00639.hp1 HG01258.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1839+2430G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983109 | ||||||
chr3:130983218
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1839+2539G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983218 | ||||||
chr3:130983239
|
A | G | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1839+2560A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983239 | ||||||
chr3:130983271
|
G | A | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1839+2592G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983271 | ||||||
chr3:130983338
|
T | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+2659T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983338 | ||||||
chr3:130983446
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+2767A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983446 | ||||||
chr3:130983657
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1839+2978C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983657 | ||||||
chr3:130983747
|
G | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+3068G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983747 | ||||||
chr3:130983799
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1839+3120C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983799 | ||||||
chr3:130983886
|
G | C | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1839+3207G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983886 | ||||||
chr3:130983908
|
C | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0313a0001c0003t0001g0369others(6): Show | 9 | HG00733.hp1 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+3229C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983908 | ||||||
chr3:130983972
|
C | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1839+3293C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130983972 | ||||||
chr3:130984004
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+3325C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984004 | ||||||
chr3:130984037
|
TG | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0006t0001g0111 | 3 | HG02055.hp2 HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+3359delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984037 | ||||||
chr3:130984243
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1839+3564T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984243 | ||||||
chr3:130984391
|
C | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(8): Show | 11 | HG00438.hp1 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.1839+3712C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984391 | ||||||
chr3:130984564
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1839+3885T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984564 | ||||||
chr3:130984624
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1839+3945A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984624 | ||||||
chr3:130984767
|
A | G | 1 | a0001c0001t0010g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1839+4088A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130984767 | ||||||
chr3:130984917
|
CAGAA | C | 44 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1839+4242_1839+424 others(8): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130984917 | |||||
chr3:130985491
|
G | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0183others(1): Show | 4 | NA18941.hp2 NA18949.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839+4812G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985491 | ||||||
chr3:130985658
|
C | CA | 49 | a0001c0001t0001g0090a0001c0001t0001g0138a0001c0001t0001g0161others(46): Show | 49 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1839+4990dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130985658 | |||||
chr3:130985664
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1839+4985A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985664 | ||||||
chr3:130985698
|
A | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02970.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1839+5019A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985698 | ||||||
chr3:130985737
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0290 | 2 | HG01243.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1839+5058A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985737 | ||||||
chr3:130985754
|
A | C | 1 | a0001c0001t0001g0314 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1839+5075A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985754 | ||||||
chr3:130985767
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1839+5088A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985767 | ||||||
chr3:130985840
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1839+5161T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985840 | ||||||
chr3:130985864
|
CG | C | 36 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(33): Show | 36 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+5186delG | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130985864 | ||||||
chr3:130986184
|
C | CT | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 265 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1839+5520dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | |||||
chr3:130986184
|
C | CTT | 43 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0095others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1839+5519_1839+552 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | |||||
chr3:130986184
|
C | CTTT | 7 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0149others(4): Show | 7 | HG00639.hp1 HG01358.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+5518_1839+552 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986184 | |||||
chr3:130986233
|
A | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1839+5554A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986233 | ||||||
chr3:130986316
|
T | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+5637T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986316 | ||||||
chr3:130986332
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1839+5653C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986332 | ||||||
chr3:130986347
|
A | G | 26 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(23): Show | 26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1839+5668A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986347 | ||||||
chr3:130986383
|
C | A | 1 | a0001c0002t0001g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1839+5704C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986383 | ||||||
chr3:130986543
|
G | A | 5 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG00438.hp2 HG02083.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1839+5864G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986543 | ||||||
chr3:130986648
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(42): Show | 46 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1839+5969A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986648 | ||||||
chr3:130986666
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0259 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1839+5987A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986666 | ||||||
chr3:130986674
|
T | C | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(320): Show | 327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.1839+5995T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986674 | ||||||
chr3:130986864
|
ATTAGT | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 48 | HG00438.hp1 HG00673.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1840-6030_1840-602 others(9): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | |||||
chr3:130986864
|
ATTAGTTT others(3): Show |
A | 16 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0025others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1840-6035_1840-602 others(14): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | |||||
chr3:130986864
|
ATTAGTTT others(8): Show |
A | 3 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0009g0076 | 3 | HG02630.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-6040_1840-602 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | |||||
chr3:130986864
|
ATTAGTTT others(13): Show |
A | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1840-6045_1840-602 others(24): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986864 | |||||
chr3:130986893
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0323 | 3 | NA18971.hp1 NA18977.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1840-6058G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130986893 | ||||||
chr3:130986893
|
GTTTAGTT others(33): Show |
G | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1840-6055_1840-601 others(44): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986893 | |||||
chr3:130986898
|
GTTTAGTT others(28): Show |
G | 22 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0103others(19): Show | 23 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1840-6050_1840-601 others(39): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986898 | |||||
chr3:130986903
|
GTTTAGTT others(23): Show |
G | 179 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1840-6045_1840-601 others(34): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986903 | |||||
chr3:130986908
|
GTTTAGTT others(18): Show |
G | 61 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 62 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1840-6040_1840-601 others(29): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986908 | |||||
chr3:130986913
|
GTTTAGTT others(13): Show |
G | 29 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0089others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1840-6035_1840-601 others(24): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986913 | |||||
chr3:130986918
|
GTTTAGTT others(8): Show |
G | 2 | a0001c0001t0001g0084a0001c0001t0001g0108 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-6030_1840-601 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130986918 | |||||
chr3:130987062
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-5889C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987062 | ||||||
chr3:130987107
|
TA | T | 7 | a0001c0001t0001g0056a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG01255.hp1 HG02056.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-5829delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130987107 | |||||
chr3:130987292
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-5659G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987292 | ||||||
chr3:130987461
|
G | A | 1 | a0001c0002t0001g0008 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1840-5490G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987461 | ||||||
chr3:130987550
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1840-5401C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987550 | ||||||
chr3:130987918
|
A | G | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-5033A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130987918 | ||||||
chr3:130988019
|
T | G | 1 | a0001c0001t0001g0001 | 3 | NA18941.hp1 NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1840-4932T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988019 | ||||||
chr3:130988330
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1840-4621G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988330 | ||||||
chr3:130988354
|
G | A | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1840-4597G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988354 | ||||||
chr3:130988560
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-4391C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988560 | ||||||
chr3:130988590
|
A | T | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-4361A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988590 | ||||||
chr3:130988591
|
T | A | 26 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(23): Show | 26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1840-4360T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988591 | ||||||
chr3:130988679
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1840-4272C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988679 | ||||||
chr3:130988748
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1840-4203G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988748 | ||||||
chr3:130988839
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1840-4112G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988839 | ||||||
chr3:130988850
|
A | G | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-4101A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988850 | ||||||
chr3:130988875
|
G | A | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-4076G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988875 | ||||||
chr3:130988971
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1840-3980G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130988971 | ||||||
chr3:130989242
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-3709C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989242 | ||||||
chr3:130989245
|
CTCAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1840-3705_1840-369 others(19): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989245 | ||||||
chr3:130989247
|
C | CA | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1840-3690dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989247 | |||||
chr3:130989247
|
C | CAA | 9 | a0001c0001t0001g0088a0001c0001t0001g0152a0001c0001t0001g0186others(6): Show | 9 | HG00280.hp1 HG01123.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1840-3691_1840-369 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989247 | |||||
chr3:130989262
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1840-3689C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989262 | ||||||
chr3:130989266
|
A | C | 1 | a0005c0008t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1840-3685A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989266 | ||||||
chr3:130989270
|
C | A | 1 | a0005c0008t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1840-3681C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989270 | ||||||
chr3:130989447
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1840-3504C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989447 | ||||||
chr3:130989489
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1840-3462C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989489 | ||||||
chr3:130989490
|
G | A | 1 | a0001c0006t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1840-3461G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989490 | ||||||
chr3:130989565
|
C | CA | 39 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0063others(36): Show | 39 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1840-3368dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | |||||
chr3:130989565
|
C | CAA | 7 | a0001c0001t0001g0044a0001c0001t0001g0147a0001c0001t0001g0157others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-3369_1840-336 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | |||||
chr3:130989565
|
C | CAAA | 7 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG02027.hp2 NA18747.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1840-3370_1840-336 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | |||||
chr3:130989565
|
CA | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 213 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1840-3368delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130989565 | |||||
chr3:130989583
|
A | C | 2 | a0001c0002t0001g0324a0001c0002t0001g0348 | 2 | NA18968.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1840-3368A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989583 | ||||||
chr3:130989592
|
C | T | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1840-3359C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989592 | ||||||
chr3:130989619
|
G | T | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1840-3332G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989619 | ||||||
chr3:130989650
|
G | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01243.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1840-3301G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989650 | ||||||
chr3:130989793
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1840-3158C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989793 | ||||||
chr3:130989916
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0170 | 2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1840-3035T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989916 | ||||||
chr3:130989955
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-2996T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130989955 | ||||||
chr3:130990070
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1840-2881T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990070 | ||||||
chr3:130990154
|
C | A | 1 | a0001c0001t0001g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1840-2797C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990154 | ||||||
chr3:130990272
|
A | AC | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1840-2668dupC | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | |||||
chr3:130990272
|
A | ACC | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 45 | HG00621.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1840-2669_1840-266 others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | |||||
chr3:130990272
|
A | ACCC | 18 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0077others(15): Show | 18 | HG00280.hp2 HG00597.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1840-2670_1840-266 others(7): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130990272 | |||||
chr3:130990310
|
A | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1840-2641A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990310 | ||||||
chr3:130990372
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0009g0076 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-2579A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990372 | ||||||
chr3:130990412
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0009g0076 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1840-2539G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990412 | ||||||
chr3:130990504
|
T | A | 30 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1840-2447T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990504 | ||||||
chr3:130990622
|
C | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1840-2329C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990622 | ||||||
chr3:130990730
|
T | C | 1 | a0001c0001t0009g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1840-2221T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990730 | ||||||
chr3:130990883
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-2068A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130990883 | ||||||
chr3:130991030
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1840-1921T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991030 | ||||||
chr3:130991203
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-1748A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991203 | ||||||
chr3:130991364
|
G | A | 1 | a0001c0001t0010g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1840-1587G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991364 | ||||||
chr3:130991514
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-1437C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991514 | ||||||
chr3:130991628
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1840-1323T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991628 | ||||||
chr3:130991671
|
T | C | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-1280T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991671 | ||||||
chr3:130991675
|
A | G | 19 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1276A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130991675 | ||||||
chr3:130992005
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1840-946C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992005 | ||||||
chr3:130992103
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1840-848A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992103 | ||||||
chr3:130992195
|
C | A | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-756C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992195 | ||||||
chr3:130992205
|
GGTACTAT others(54): Show |
G | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1840-682_1840-622d others(63): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr3 | 130992205 | |||||
chr3:130992341
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1840-610A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992341 | ||||||
chr3:130992613
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1840-338G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992613 | ||||||
chr3:130992735
|
G | A | 24 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-216G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992735 | ||||||
chr3:130992806
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1840-145T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 20/27 | chr3 | 130992806 | ||||||
chr3:130993079
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1890+78A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993079 | ||||||
chr3:130993091
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0174others(28): Show | 32 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1890+90A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993091 | ||||||
chr3:130993120
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0038others(1): Show | 4 | HG00438.hp1 HG00673.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890+119C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993120 | ||||||
chr3:130993122
|
G | GT | 8 | a0001c0001t0001g0044a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG01255.hp1 HG02135.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1890+133dupT | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr3 | 130993122 | |||||
chr3:130993123
|
T | TG | 20 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0028others(17): Show | 22 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1890+122_1890+123i others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993123 | ||||||
chr3:130993311
|
G | C | 1 | a0001c0001t0001g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1890+310G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 21/27 | chr3 | 130993311 | ||||||
chr3:130994116
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2057+18G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994116 | ||||||
chr3:130994138
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2057+40C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994138 | ||||||
chr3:130994370
|
G | A | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2057+272G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994370 | ||||||
chr3:130994494
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2057+396G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994494 | ||||||
chr3:130994571
|
T | G | 1 | a0001c0001t0001g0356 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2057+473T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994571 | ||||||
chr3:130994598
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2057+500T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994598 | ||||||
chr3:130994599
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0056 | 2 | HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2057+501A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994599 | ||||||
chr3:130994601
|
A | G | 2 | a0003c0005t0003g0100a0003c0005t0003g0101 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2057+503A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994601 | ||||||
chr3:130994648
|
C | CATTT | 7 | a0001c0001t0001g0222a0001c0001t0001g0245a0001c0001t0001g0301others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2057+567_2057+570d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr3 | 130994648 | |||||
chr3:130994655
|
T | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052 | 3 | HG00099.hp1 HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2057+557T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994655 | ||||||
chr3:130994798
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2057+700A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130994798 | ||||||
chr3:130995059
|
A | T | 26 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(23): Show | 26 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2057+961A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995059 | ||||||
chr3:130995380
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 298 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2058-663G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995380 | ||||||
chr3:130995398
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2058-645G>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995398 | ||||||
chr3:130995419
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2058-624A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995419 | ||||||
chr3:130995637
|
T | TTTTA | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2058-398_2058-395d others(6): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr3 | 130995637 | |||||
chr3:130995744
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2058-299G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995744 | ||||||
chr3:130995790
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2058-253G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995790 | ||||||
chr3:130995801
|
C | T | 4 | a0002c0004t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058-242C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995801 | ||||||
chr3:130995886
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2058-157C>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995886 | ||||||
chr3:130995896
|
C | T | 1 | a0001c0002t0001g0008 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2058-147C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130995896 | ||||||
chr3:130996023
|
C | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2058-20C>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130996023 | ||||||
chr3:130996026
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0229 | 2 | HG00621.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2058-17T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 22/27 | chr3 | 130996026 | ||||||
chr3:130996224
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2126+113A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996224 | ||||||
chr3:130996571
|
T | G | 45 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2127-109T>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996571 | ||||||
chr3:130996612
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2127-68A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 23/27 | chr3 | 130996612 | ||||||
chr3:130996904
|
A | C | 31 | a0001c0002t0001g0215a0001c0002t0001g0231a0001c0002t0001g0315others(28): Show | 31 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.2243+108A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996904 | ||||||
chr3:130996931
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2243+135G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996931 | ||||||
chr3:130996970
|
A | G | 44 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2243+174A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130996970 | ||||||
chr3:130997020
|
G | A | 1 | a0001c0002t0001g0328 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2243+224G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997020 | ||||||
chr3:130997194
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2243+398T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997194 | ||||||
chr3:130997325
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2244-281C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 24/27 | chr3 | 130997325 | ||||||
chr3:130997811
|
CTTAG | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2391+62_2391+65del others(4): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr3 | 130997811 | |||||
chr3:130997951
|
C | T | 1 | a0001c0002t0001g0318 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2391+198C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130997951 | ||||||
chr3:130998076
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 9 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2392-218A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998076 | ||||||
chr3:130998128
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2392-166A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998128 | ||||||
chr3:130998148
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2392-146G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 25/27 | chr3 | 130998148 | ||||||
chr3:130998677
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 8 | HG01243.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2487+288A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998677 | ||||||
chr3:130998703
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2487+314T>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998703 | ||||||
chr3:130998752
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0136 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2487+363A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998752 | ||||||
chr3:130998787
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2487+398C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998787 | ||||||
chr3:130998866
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2487+477C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130998866 | ||||||
chr3:130999029
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2488-489A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999029 | ||||||
chr3:130999052
|
G | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01255.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2488-466G>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999052 | ||||||
chr3:130999065
|
T | C | 16 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(13): Show | 16 | HG00609.hp2 HG02074.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.2488-453T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999065 | ||||||
chr3:130999312
|
A | T | 39 | a0001c0002t0001g0008a0001c0002t0001g0215a0001c0002t0001g0231others(36): Show | 39 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2488-206A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 26/27 | chr3 | 130999312 | ||||||
chr3:130999715
|
A | C | 1 | a0001c0001t0006g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2629+56A>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 130999715 | ||||||
chr3:131000205
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2629+546G>A | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000205 | ||||||
chr3:131000375
|
A | G | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01884.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2629+716A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000375 | ||||||
chr3:131000391
|
A | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2629+732A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000391 | ||||||
chr3:131000452
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2630-768A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000452 | ||||||
chr3:131000460
|
T | C | 44 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(41): Show | 44 | HG00597.hp2 HG01081.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.2630-760T>C | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000460 | ||||||
chr3:131000529
|
A | G | 1 | a0001c0002t0001g0335 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2630-691A>G | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000529 | ||||||
chr3:131000555
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2630-665C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000555 | ||||||
chr3:131000595
|
TA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2630-624delA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000595 | ||||||
chr3:131000645
|
A | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2630-575A>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000645 | ||||||
chr3:131000948
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2630-272C>T | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | chr3 | 131000948 | ||||||
chr3:131001104
|
G | GA | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.2630-93dupA | ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 | |||||
chr3:131001104
|
G | GAA | 36 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0102others(33): Show | 37 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2630-94_2630-93dup others(2): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 | |||||
chr3:131001104
|
G | GAAA | 12 | a0001c0001t0001g0088a0001c0001t0001g0105a0001c0001t0001g0113others(9): Show | 12 | HG01169.hp1 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2630-95_2630-93dup others(3): Show |
ATP2C1 | ENSG00000017260.20 | transcript | ENST00000510168.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr3 | 131001104 |