geneid | 6102 |
---|---|
ensemblid | ENSG00000102218.6 |
hgncid | 10274 |
symbol | RP2 |
name | RP2 activator of ARL3 GTPase |
refseq_nuc | NM_006915.3 |
refseq_prot | NP_008846.2 |
ensembl_nuc | ENST00000218340.4 |
ensembl_prot | ENSP00000218340.3 |
mane_status | MANE Select |
chr | chrX |
start | 46837043 |
end | 46882358 |
strand | + |
ver | v1.2 |
region | chrX:46837043-46882358 |
region5000 | chrX:46832043-46887358 |
regionname0 | RP2_chrX_46837043_46882358 |
regionname5000 | RP2_chrX_46832043_46887358 |
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 | 350 | 269 | 75 | 45 | 114 | 10 | 23 | 87 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0002 | 0/0 | 350 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0003 | 0/0 | 350 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0004 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0005 | 0/0 | 67 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
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 | 1053 | 268 | 74 | 45 | 114 | 10 | 23 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
c0002 | 0/0 | 1053 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
c0003 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
c0004 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
c0005 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
c0006 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2648 | 240 | 57 | 43 | 106 | 11 | 22 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0002 | 1/0 | 2648 | 16 | 10 | 0 | 5 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0003 | 0/0 | 2648 | 6 | 6 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0004 | 0/0 | 2651 | 3 | 2 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0005 | 0/0 | 2647 | 2 | 0 | 0 | 0 | 0 | 2 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0006 | 0/0 | 2648 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0007 | 0/0 | 2647 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0008 | 0/0 | 2648 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0009 | 0/0 | 2648 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0010 | 0/0 | 2648 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
t0011 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
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 | 10 | 0 | 1 | 8 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0006 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
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 | 1053 | 268 | 74 | 45 | 114 | 10 | 23 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0003 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0002c0002 | 0/0 | 1053 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0003c0004 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0004c0005 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0005c0006 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3700 | 234 | 55 | 43 | 104 | 10 | 21 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0002 | 1/0 | 3700 | 16 | 10 | 0 | 5 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0003 | 0/0 | 3700 | 6 | 6 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0004 | 0/0 | 3703 | 3 | 2 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0005 | 0/0 | 3699 | 2 | 0 | 0 | 0 | 0 | 2 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0006 | 0/0 | 3700 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0007 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0008 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0009 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0010 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0001t0011 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0001c0003t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0002c0002t0001 | 0/0 | 3700 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0003c0004t0001 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0004c0005t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
a0005c0006t0001 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | copy fasta | chrX | 46832043 | 46887358 |
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 | 9 | 0 | 1 | 7 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0008g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0003c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0004c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
a0005c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02083 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0201 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02300 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02717 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0028 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02965 | hp1 | a0004 | c0005 | t0001 | g0111 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18961 | hp1 | a0005 | c0006 | t0001 | g0083 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18971 | hp1 | a0003 | c0004 | t0001 | g0025 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0145 | REF | REF | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0076 | REF | REF | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:46853556
|
G | GT | 1 | a0005 | 1 | NA18961.hp1 | frameshift_variant | HIGH | c.186dupT | p.Leu63fs | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 245/3700 | 187/1053 | 63/350 | INFO_REALIGN_3_PRIME | chrX | 46853556 | |
chrX:46853583
|
T | TA | 1 | a0005 | 1 | NA18961.hp1 | frameshift_variant | HIGH | c.212dupA | p.Asn71fs | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 271/3700 | 213/1053 | 71/350 | INFO_REALIGN_3_PRIME | chrX | 46853583 | |
chrX:46853614
|
G | GT | 1 | a0005 | 1 | NA18961.hp1 | frameshift_variant | HIGH | c.243dupT | p.Thr82fs | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 302/3700 | 244/1053 | 82/350 | INFO_REALIGN_3_PRIME | chrX | 46853614 | |
chrX:46853974
|
A | G | 1 | a0004 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.601A>G | p.Ile201Val | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 659/3700 | 601/1053 | 201/350 | chrX | 46853974 | ||
chrX:46853977
|
C | CCTA | 1 | a0005 | 1 | NA18961.hp1 | disruptive_inframe_insertion | MODERATE | c.609_611dupTAC | p.Thr204dup | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 670/3700 | 612/1053 | 204/350 | INFO_REALIGN_3_PRIME | chrX | 46853977 | |
chrX:46854041
|
T | TA | 1 | a0005 | 1 | NA18961.hp1 | frameshift_variant | HIGH | c.669dupA | p.Ser224fs | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 728/3700 | 670/1053 | 224/350 | INFO_REALIGN_3_PRIME | chrX | 46854041 | |
chrX:46860033
|
A | G | 1 | a0003 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.814A>G | p.Met272Val | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/5 | 872/3700 | 814/1053 | 272/350 | chrX | 46860033 | ||
chrX:46860063
|
C | T | 1 | a0002 | 2 | HG01516.hp1 HG03017.hp1 |
missense_variant | MODERATE | c.844C>T | p.Arg282Trp | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/5 | 902/3700 | 844/1053 | 282/350 | chrX | 46860063 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:46853979
|
T | C | 1 | a0001c0003 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.606T>C | p.Pro202Pro | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 664/3700 | 606/1053 | 202/350 | chrX | 46853979 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:46880204
|
C | T | 1 | a0001c0001t0011 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 435 | chrX | 46880204 | |||||
chrX:46880575
|
CT | C | 1 | a0001c0001t0005 | 2 | HG02735.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 808 | INFO_REALIGN_3_PRIME | chrX | 46880575 | ||||
chrX:46880597
|
G | A | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 828 | chrX | 46880597 | |||||
chrX:46880673
|
A | G | 1 | a0001c0001t0010 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 904 | chrX | 46880673 | |||||
chrX:46880701
|
A | G | 1 | a0001c0001t0009 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 932 | chrX | 46880701 | |||||
chrX:46881008
|
AT | A | 1 | a0001c0001t0007 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 1244 | INFO_REALIGN_3_PRIME | chrX | 46881008 | ||||
chrX:46881256
|
C | A | 1 | a0001c0001t0008 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 1487 | chrX | 46881256 | |||||
chrX:46881463
|
A | ATAT | 1 | a0001c0001t0004 | 3 | HG02486.hp1 HG02886.hp2 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1717_*1719dupATT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 1720 | INFO_REALIGN_3_PRIME | chrX | 46881463 | ||||
chrX:46881854
|
T | C | 1 | a0001c0001t0003 | 6 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 2085 | chrX | 46881854 | |||||
chrX:46881925
|
A | G | 1 | a0001c0001t0006 | 2 | HG00558.hp1 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2156A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 2156 | chrX | 46881925 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:46837230
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102+28C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837230 | ||||||
chrX:46837258
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.102+56C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837258 | ||||||
chrX:46837279
|
A | AG | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+82dupG | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46837279 | |||||
chrX:46837354
|
A | AG | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+153dupG | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46837354 | |||||
chrX:46837624
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.102+422G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837624 | ||||||
chrX:46837667
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+465T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837667 | ||||||
chrX:46837668
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+466C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837668 | ||||||
chrX:46837669
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+467T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837669 | ||||||
chrX:46837709
|
G | GA | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+508dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46837709 | |||||
chrX:46837758
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+556G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837758 | ||||||
chrX:46837768
|
A | AC | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+567dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46837768 | |||||
chrX:46837812
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.102+610G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837812 | ||||||
chrX:46837975
|
A | AC | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+773_102+774ins others(1): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837975 | ||||||
chrX:46837980
|
AC | A | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+779delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837980 | ||||||
chrX:46837984
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.102+782G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837984 | ||||||
chrX:46837987
|
C | CT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+785_102+786ins others(1): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837987 | ||||||
chrX:46837992
|
AT | A | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+793delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46837992 | |||||
chrX:46838003
|
G | GT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+803dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838003 | |||||
chrX:46838095
|
CA | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+896delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838095 | |||||
chrX:46838205
|
A | AT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1006dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838205 | |||||
chrX:46838302
|
CT | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1103delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838302 | |||||
chrX:46838427
|
A | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+1225A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838427 | ||||||
chrX:46838429
|
GA | G | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1229delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838429 | |||||
chrX:46838560
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1358T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838560 | ||||||
chrX:46838616
|
C | CT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1420dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838616 | |||||
chrX:46838656
|
GT | G | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1457delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838656 | |||||
chrX:46838774
|
C | CT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1576dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838774 | |||||
chrX:46838903
|
C | CT | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1710dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838903 | |||||
chrX:46838903
|
CT | C | 1 | a0001c0001t0001g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.102+1710delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46838903 | |||||
chrX:46838946
|
GT | G | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1745delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838946 | ||||||
chrX:46838957
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0004g0033 | 3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+1755T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838957 | ||||||
chrX:46839098
|
CT | C | 2 | a0001c0001t0003g0034a0001c0001t0004g0035 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.102+1897delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839098 | ||||||
chrX:46839167
|
C | CT | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1970dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46839167 | |||||
chrX:46839174
|
G | GT | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+1981dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46839174 | |||||
chrX:46839281
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.102+2079G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839281 | ||||||
chrX:46839335
|
T | G | 4 | a0001c0001t0003g0010a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+2133T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839335 | ||||||
chrX:46839507
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102+2305G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839507 | ||||||
chrX:46839561
|
A | AT | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+2359_102+2360i others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839561 | ||||||
chrX:46839561
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(76): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.102+2359A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839561 | ||||||
chrX:46839967
|
G | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | NA18972.hp1 NA19001.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.102+2765G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839967 | ||||||
chrX:46839987
|
CT | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+2790delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46839987 | |||||
chrX:46839993
|
G | A | 1 | a0001c0003t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+2791G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839993 | ||||||
chrX:46840151
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.102+2949T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840151 | ||||||
chrX:46840199
|
T | G | 1 | a0001c0001t0003g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.102+2997T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840199 | ||||||
chrX:46840368
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(67): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.102+3166A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840368 | ||||||
chrX:46840784
|
T | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+3582T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840784 | ||||||
chrX:46840868
|
CAT | C | 1 | a0001c0001t0004g0217 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.102+3667_102+3668d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840868 | ||||||
chrX:46840889
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102+3687T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840889 | ||||||
chrX:46841229
|
ACAGT | A | 1 | a0001c0001t0002g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.102+4028_102+4031d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841229 | ||||||
chrX:46841237
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.102+4035G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841237 | ||||||
chrX:46841424
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.102+4222G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841424 | ||||||
chrX:46841425
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.102+4223C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841425 | ||||||
chrX:46841426
|
AGGGT | A | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.102+4225_102+4228d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841426 | ||||||
chrX:46842146
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0159others(3): Show | 7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+4944C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842146 | ||||||
chrX:46842363
|
A | G | 1 | a0001c0001t0004g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+5161A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842363 | ||||||
chrX:46842401
|
A | G | 1 | a0001c0001t0004g0217 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.102+5199A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842401 | ||||||
chrX:46842966
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0225 | 3 | NA19001.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.102+5764G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842966 | ||||||
chrX:46843005
|
C | CT | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG01192.hp1 HG01261.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+5823dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46843005 | |||||
chrX:46843005
|
CT | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0052others(6): Show | 10 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+5823delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46843005 | |||||
chrX:46843096
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102+5894C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843096 | ||||||
chrX:46843269
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.102+6067A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843269 | ||||||
chrX:46843310
|
G | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6108G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843310 | ||||||
chrX:46843453
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+6251G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843453 | ||||||
chrX:46843548
|
C | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.102+6346C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843548 | ||||||
chrX:46843780
|
G | GTATATAA others(28): Show |
1 | a0001c0001t0001g0145 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.102+6597_102+6631d others(37): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46843780 | |||||
chrX:46843925
|
C | T | 2 | a0001c0001t0003g0034a0001c0001t0004g0035 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.102+6723C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843925 | ||||||
chrX:46844184
|
A | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0225 | 3 | NA19001.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.102+6982A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844184 | ||||||
chrX:46844409
|
A | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+7207A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844409 | ||||||
chrX:46844641
|
A | G | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.102+7439A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844641 | ||||||
chrX:46844847
|
C | G | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.102+7645C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844847 | ||||||
chrX:46845770
|
G | GT | 5 | a0001c0001t0001g0144a0001c0001t0001g0215a0001c0001t0002g0156others(2): Show | 5 | HG02109.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-7695dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46845770 | |||||
chrX:46845968
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.103-7508G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46845968 | ||||||
chrX:46846009
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.103-7467G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46846009 | ||||||
chrX:46846828
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.103-6648A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46846828 | ||||||
chrX:46847025
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-6451C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847025 | ||||||
chrX:46847093
|
C | CT | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.103-6381dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847093 | |||||
chrX:46847493
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.103-5983C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847493 | ||||||
chrX:46847497
|
C | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0140 | 5 | NA18960.hp1 NA18992.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5979C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847497 | ||||||
chrX:46847630
|
G | C | 1 | a0001c0001t0002g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.103-5846G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847630 | ||||||
chrX:46847668
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-5808A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847668 | ||||||
chrX:46847687
|
T | TATATATG others(21): Show |
1 | a0001c0001t0001g0021 | 2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.103-5767_103-5740d others(30): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847687 | |||||
chrX:46847692
|
ATG | A | 2 | a0001c0001t0003g0034a0001c0001t0004g0035 | 2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.103-5774_103-5773d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847692 | |||||
chrX:46847704
|
A | ATATACAC others(13): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062 | 3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5768_103-5767i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847704 | |||||
chrX:46847709
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.103-5767T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847709 | ||||||
chrX:46847711
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062 | 3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5765C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847711 | ||||||
chrX:46847715
|
CAT | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 7 | HG02717.hp1 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-5756_103-5755d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847715 | |||||
chrX:46847716
|
A | C | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5760A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847716 | ||||||
chrX:46847717
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062 | 3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5759T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847717 | ||||||
chrX:46847717
|
T | TATATGTG others(15): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0214 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.103-5747_103-5746i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | |||||
chrX:46847717
|
T | TATATGTG others(17): Show |
25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(22): Show | 31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.103-5732_103-5709d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | |||||
chrX:46847717
|
T | TATATGTG others(41): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0175 | 2 | HG01943.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.103-5756_103-5709d others(50): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | |||||
chrX:46847719
|
T | TATGTGTG others(63): Show |
1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(72): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847719 | |||||
chrX:46847720
|
ATG | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 8 | HG00323.hp1 HG01123.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-5746_103-5745d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847720 | |||||
chrX:46847721
|
T | TGTGTGTG others(61): Show |
1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(70): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847721 | |||||
chrX:46847722
|
G | GTGTGTGT others(13): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5747_103-5746i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | |||||
chrX:46847722
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0164 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.103-5752_103-5733d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | |||||
chrX:46847722
|
G | GTGTGTGT others(15): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0160others(1): Show | 5 | HG02258.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5744_103-5723d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | |||||
chrX:46847733
|
TATACACA others(39): Show |
T | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0061 | 5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5732_103-5687d others(48): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847733 | |||||
chrX:46847735
|
T | TAC | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.103-5735_103-5734d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847735 | |||||
chrX:46847741
|
CAT | C | 9 | a0001c0001t0001g0136a0001c0001t0002g0138a0001c0001t0002g0139others(6): Show | 10 | HG02109.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-5732_103-5731d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847741 | |||||
chrX:46847742
|
ATATG | A | 5 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0156others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5732_103-5729d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847742 | |||||
chrX:46847743
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0002g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.103-5733_103-5732i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847743 | ||||||
chrX:46847743
|
TATGTGTG others(15): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.103-5719_103-5698d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847743 | |||||
chrX:46847744
|
A | G | 5 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5732A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847744 | ||||||
chrX:46847744
|
ATG | A | 2 | a0001c0001t0001g0162a0001c0001t0003g0036 | 2 | HG01934.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.103-5722_103-5721d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847744 | |||||
chrX:46847744
|
ATGTGTGT others(17): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103-5722_103-5699d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847744 | |||||
chrX:46847745
|
T | TGTGTGTG others(33): Show |
1 | a0001c0001t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.103-5723_103-5722i others(42): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847745 | |||||
chrX:46847745
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.103-5730_103-5711d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847745 | |||||
chrX:46847752
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5724G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847752 | ||||||
chrX:46847754
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5722G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847754 | ||||||
chrX:46847754
|
G | GTA | 1 | a0001c0001t0001g0132 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.103-5717_103-5716d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847754 | |||||
chrX:46847757
|
TATACACA others(15): Show |
T | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-5697_103-5676d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847757 | |||||
chrX:46847758
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-5718A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847758 | ||||||
chrX:46847765
|
C | CAT | 4 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG00609.hp1 NA18747.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-5710_103-5709d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847765 | |||||
chrX:46847765
|
C | CATAT | 1 | a0001c0001t0005g0027 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847765 | |||||
chrX:46847765
|
CAT | C | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.103-5710_103-5709d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847765 | ||||||
chrX:46847766
|
A | ATATG | 1 | a0001c0001t0005g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847766 | |||||
chrX:46847766
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(28): Show | 38 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.103-5710A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847766 | ||||||
chrX:46847766
|
ATG | A | 1 | a0001c0001t0001g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.103-5700_103-5699d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847766 | |||||
chrX:46847767
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.103-5709T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847767
|
T | TATGTGTG others(13): Show |
1 | a0001c0001t0001g0172 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.103-5709_103-5708i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847767
|
T | TATGTGTG others(15): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(23): Show | 33 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-5709_103-5708i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847767
|
T | TATGTGTG others(59): Show |
1 | a0001c0001t0001g0180 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(68): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847767
|
T | TATGTGTG others(15): Show |
2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.103-5709_103-5708i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847767
|
TGTGTGTG others(13): Show |
T | 13 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0159others(10): Show | 14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-5708_103-5689d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | ||||||
chrX:46847768
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0170a0001c0001t0001g0171others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-5708G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847768 | ||||||
chrX:46847770
|
G | A | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5706G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847770 | ||||||
chrX:46847775
|
TGTAC | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5700_103-5697d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847775 | ||||||
chrX:46847776
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(36): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.103-5700G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847776 | ||||||
chrX:46847776
|
G | GTATA | 2 | a0001c0001t0001g0042a0001c0001t0002g0139 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.103-5698_103-5697i others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847776 | |||||
chrX:46847776
|
G | GTGTATA | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.103-5699_103-5698i others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847776 | |||||
chrX:46847779
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(111): Show | 137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.103-5697C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847779 | ||||||
chrX:46847781
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(36): Show | 47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.103-5695T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847781 | ||||||
chrX:46847781
|
T | TATATAC | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 6 | HG01081.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5694_103-5693i others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847781 | |||||
chrX:46847783
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5693C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847783 | ||||||
chrX:46847784
|
A | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5692A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847784 | ||||||
chrX:46847785
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5691C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847785 | ||||||
chrX:46847786
|
A | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5690A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847786 | ||||||
chrX:46847787
|
C | CAT | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(42): Show | 52 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.103-5688_103-5687d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847787 | |||||
chrX:46847787
|
C | CATATGTG others(41): Show |
1 | a0001c0001t0001g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.103-5687_103-5686i others(50): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847787 | |||||
chrX:46847787
|
C | CGTGTGTG others(13): Show |
3 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | NA18747.hp1 NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.103-5689_103-5688i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | ||||||
chrX:46847787
|
C | CGTGTGTG others(15): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0173others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-5689_103-5688i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | ||||||
chrX:46847787
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(44): Show | 56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.103-5689C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | ||||||
chrX:46847787
|
CAT | C | 1 | a0001c0001t0001g0017 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.103-5688_103-5687d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | ||||||
chrX:46847788
|
A | ATATATG | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-5687_103-5686i others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | |||||
chrX:46847788
|
A | ATATATGT others(175): Show |
1 | a0001c0001t0005g0027 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.103-5687_103-5686i others(184): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | |||||
chrX:46847788
|
A | ATATATGT others(173): Show |
1 | a0001c0001t0005g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.103-5687_103-5686i others(182): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | |||||
chrX:46847788
|
A | ATG | 1 | a0001c0001t0001g0059 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.103-5678_103-5677d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | |||||
chrX:46847788
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.103-5688A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847788 | ||||||
chrX:46847790
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0130others(9): Show | 14 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.103-5686G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847790 | ||||||
chrX:46847792
|
G | A | 6 | a0001c0001t0002g0139a0001c0001t0002g0156a0001c0001t0002g0157others(3): Show | 6 | HG02109.hp2 HG02735.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5684G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847792 | ||||||
chrX:46847794
|
G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0171 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.103-5679_103-5678i others(28): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847794 | |||||
chrX:46847798
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5678G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847798 | ||||||
chrX:46847798
|
GTATA | G | 2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.103-5671_103-5668d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847798 | |||||
chrX:46847802
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5674A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847802 | ||||||
chrX:46847804
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5672A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847804 | ||||||
chrX:46847806
|
A | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5670A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847806 | ||||||
chrX:46847807
|
TACAC | T | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5665_103-5662d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847807 | |||||
chrX:46847808
|
A | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5668A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847808 | ||||||
chrX:46847809
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5667C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847809 | ||||||
chrX:46847811
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5665C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847811 | ||||||
chrX:46847813
|
C | T | 4 | a0001c0001t0002g0139a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5663C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847813 | ||||||
chrX:46847813
|
CAT | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.103-5658_103-5657d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847813 | |||||
chrX:46847816
|
A | G | 4 | a0001c0001t0002g0139a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5660A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847816 | ||||||
chrX:46847818
|
A | G | 4 | a0001c0001t0002g0139a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5658A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847818 | ||||||
chrX:46847822
|
G | A | 4 | a0001c0001t0002g0139a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5654G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847822 | ||||||
chrX:46847822
|
G | GTATATGT others(15): Show |
4 | a0001c0001t0002g0137a0001c0001t0002g0138a0001c0001t0002g0141others(1): Show | 4 | HG02622.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5632_103-5611d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847822 | |||||
chrX:46847822
|
G | GTATATGT others(37): Show |
2 | a0001c0001t0002g0134a0001c0001t0002g0135 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.103-5611_103-5610i others(46): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847822 | |||||
chrX:46847824
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-5652A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847824 | ||||||
chrX:46847826
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-5650A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847826 | ||||||
chrX:46847901
|
T | C | 4 | a0001c0001t0003g0010a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5575T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847901 | ||||||
chrX:46847913
|
CAT | C | 2 | a0001c0001t0004g0035a0001c0001t0006g0212 | 2 | HG02886.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.103-5558_103-5557d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847913 | |||||
chrX:46847929
|
C | CAT | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103-5520_103-5519d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | |||||
chrX:46847929
|
CAT | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(65): Show | 83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.103-5520_103-5519d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | |||||
chrX:46847929
|
CATAT | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.103-5522_103-5519d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | |||||
chrX:46847929
|
CATATAT | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0042others(26): Show | 32 | HG01081.hp2 HG01123.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.103-5524_103-5519d others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | |||||
chrX:46848123
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.103-5353C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848123 | ||||||
chrX:46848196
|
C | G | 1 | a0001c0001t0011g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-5280C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848196 | ||||||
chrX:46848384
|
A | AT | 9 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0067others(6): Show | 9 | HG02055.hp1 HG02129.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-5075dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46848384 | |||||
chrX:46848384
|
AT | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0110 | 2 | HG03688.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.103-5075delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46848384 | |||||
chrX:46848448
|
G | A | 4 | a0001c0001t0003g0010a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5028G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848448 | ||||||
chrX:46848454
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.103-5022G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848454 | ||||||
chrX:46848519
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.103-4957A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848519 | ||||||
chrX:46848689
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(81): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.103-4787C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848689 | ||||||
chrX:46848734
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103-4742A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848734 | ||||||
chrX:46849039
|
A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-4437A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849039 | ||||||
chrX:46849161
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.103-4315C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849161 | ||||||
chrX:46849193
|
C | CT | 2 | a0001c0001t0001g0109a0001c0001t0001g0198 | 2 | NA19006.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.103-4271dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46849193 | |||||
chrX:46849193
|
CT | C | 1 | a0004c0005t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.103-4271delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46849193 | |||||
chrX:46849282
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-4194C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849282 | ||||||
chrX:46849377
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-4099C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849377 | ||||||
chrX:46849830
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.103-3640dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46849830 | |||||
chrX:46850049
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.103-3427G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46850049 | ||||||
chrX:46850691
|
ATCCATTC others(13): Show |
A | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-2784_103-2765d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46850691 | ||||||
chrX:46851001
|
A | AT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-2473dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851001 | |||||
chrX:46851044
|
T | TA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-2428dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851044 | |||||
chrX:46851088
|
AT | A | 10 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0137others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-2385delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851088 | |||||
chrX:46851258
|
C | CA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-2213dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851258 | |||||
chrX:46851386
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(95): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.103-2090C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851386 | ||||||
chrX:46851555
|
G | GA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-1919dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851555 | |||||
chrX:46851560
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-1916C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851560 | ||||||
chrX:46851620
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-1856G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851620 | ||||||
chrX:46851629
|
TC | T | 1 | a0001c0001t0001g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.103-1845delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851629 | |||||
chrX:46851695
|
GC | G | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-1779delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851695 | |||||
chrX:46851697
|
C | T | 1 | a0001c0001t0003g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103-1779C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851697 | ||||||
chrX:46851792
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103-1684C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851792 | ||||||
chrX:46851838
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0147 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.103-1638G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851838 | ||||||
chrX:46851983
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-1493C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851983 | ||||||
chrX:46852022
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.103-1454G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852022 | ||||||
chrX:46852065
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0159others(3): Show | 7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-1411G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852065 | ||||||
chrX:46852256
|
A | AAGGG | 1 | a0001c0001t0001g0197 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.103-1208_103-1205d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46852256 | |||||
chrX:46852263
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0085a0001c0001t0001g0224 | 3 | NA18952.hp1 NA19010.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.103-1213G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852263 | ||||||
chrX:46852275
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG04204.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.103-1201G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852275 | ||||||
chrX:46852359
|
G | GA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-1114dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46852359 | |||||
chrX:46852422
|
A | AT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-1051dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46852422 | |||||
chrX:46852546
|
CA | C | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103-929delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852546 | ||||||
chrX:46852580
|
T | TTTA | 1 | a0001c0001t0001g0041 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.103-881_103-879dup others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46852580 | |||||
chrX:46852924
|
C | CA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-546dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46852924 | |||||
chrX:46853206
|
C | CT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-267dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46853206 | |||||
chrX:46853232
|
A | AT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-241dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46853232 | |||||
chrX:46853258
|
T | TC | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-217dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46853258 | |||||
chrX:46853412
|
T | TC | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-62dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46853412 | |||||
chrX:46853461
|
G | GT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-11dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46853461 | |||||
chrX:46854182
|
T | TA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768+46dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854182 | |||||
chrX:46854241
|
G | GC | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768+101dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854241 | |||||
chrX:46854271
|
A | AC | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.768+135dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854271 | |||||
chrX:46854429
|
T | TA | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768+295dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854429 | |||||
chrX:46854609
|
T | TA | 12 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.768+469dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854609 | |||||
chrX:46854771
|
A | AT | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768+642dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854771 | |||||
chrX:46854790
|
G | T | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+649G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46854790 | ||||||
chrX:46854797
|
G | GC | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768+657dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854797 | |||||
chrX:46855153
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0084others(2): Show | 5 | HG00099.hp1 HG01106.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1012C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855153 | ||||||
chrX:46855228
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.768+1087T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855228 | ||||||
chrX:46855259
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.768+1118T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855259 | ||||||
chrX:46855445
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.768+1304G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855445 | ||||||
chrX:46855797
|
A | AT | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(98): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.768+1668dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46855797 | |||||
chrX:46855797
|
A | ATT | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.768+1667_768+1668d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46855797 | |||||
chrX:46856155
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(130): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.768+2014G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856155 | ||||||
chrX:46856196
|
A | C | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+2055A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856196 | ||||||
chrX:46856501
|
CA | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | NA18966.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.768+2362delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46856501 | |||||
chrX:46856702
|
C | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+2561C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856702 | ||||||
chrX:46856900
|
CTTATATA | C | 1 | a0001c0001t0011g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.768+2766_768+2772d others(9): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46856900 | |||||
chrX:46857138
|
A | AT | 22 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(19): Show | 23 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.769-2838dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46857138 | |||||
chrX:46857138
|
A | ATT | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.769-2839_769-2838d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46857138 | |||||
chrX:46857328
|
G | A | 3 | a0001c0001t0002g0137a0001c0001t0002g0138a0001c0001t0002g0152 | 3 | HG02622.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.769-2660G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46857328 | ||||||
chrX:46857597
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0061 | 5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-2391G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46857597 | ||||||
chrX:46857654
|
A | AATTGTTT others(2): Show |
2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.769-2334_769-2333i others(11): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46857654 | ||||||
chrX:46858474
|
A | AT | 8 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 9 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.769-1501dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46858474 | |||||
chrX:46858474
|
AT | A | 1 | a0001c0001t0001g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.769-1501delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46858474 | |||||
chrX:46858644
|
A | AT | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062 | 3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.769-1335dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46858644 | |||||
chrX:46858667
|
C | A | 13 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0061others(10): Show | 15 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.769-1321C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46858667 | ||||||
chrX:46858736
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.769-1252G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46858736 | ||||||
chrX:46858883
|
AT | A | 1 | a0001c0001t0002g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.769-1103delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46858883 | |||||
chrX:46859217
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769-771T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859217 | ||||||
chrX:46859318
|
C | CA | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.769-662dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46859318 | |||||
chrX:46859327
|
T | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.769-661T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859327 | ||||||
chrX:46859488
|
C | CA | 7 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0062others(4): Show | 9 | HG01255.hp1 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-485dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46859488 | |||||
chrX:46859488
|
CA | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0001t0001g0071others(8): Show | 11 | HG01891.hp1 HG01928.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.769-485delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46859488 | |||||
chrX:46859569
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.769-419T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859569 | ||||||
chrX:46859776
|
A | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.769-212A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859776 | ||||||
chrX:46860267
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.883+165G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860267 | ||||||
chrX:46860277
|
C | T | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.883+175C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860277 | ||||||
chrX:46860391
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.883+289C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860391 | ||||||
chrX:46860478
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.883+376T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860478 | ||||||
chrX:46860522
|
AT | A | 1 | a0001c0001t0001g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.883+424delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46860522 | |||||
chrX:46860637
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.883+535A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860637 | ||||||
chrX:46860666
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.883+564T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860666 | ||||||
chrX:46860960
|
AAGTATTA others(4): Show |
A | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.883+865_883+875del others(11): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46860960 | |||||
chrX:46861221
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.883+1119C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861221 | ||||||
chrX:46861229
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.883+1127C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861229 | ||||||
chrX:46861271
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.883+1169G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861271 | ||||||
chrX:46861360
|
CA | C | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+1263delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46861360 | |||||
chrX:46861367
|
T | C | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+1265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861367 | ||||||
chrX:46861377
|
AC | A | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+1277delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46861377 | |||||
chrX:46861581
|
A | AC | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.883+1483dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46861581 | |||||
chrX:46861591
|
TC | T | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+1492delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46861591 | |||||
chrX:46861768
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+1666G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861768 | ||||||
chrX:46861770
|
G | GC | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+1669dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46861770 | |||||
chrX:46861772
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+1670T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861772 | ||||||
chrX:46861797
|
T | C | 4 | a0001c0001t0003g0010a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+1695T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861797 | ||||||
chrX:46861835
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883+1733T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861835 | ||||||
chrX:46862006
|
AC | A | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.883+1908delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46862006 | |||||
chrX:46862145
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883+2043G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862145 | ||||||
chrX:46862388
|
T | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0159others(3): Show | 7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+2286T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862388 | ||||||
chrX:46862412
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883+2310A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862412 | ||||||
chrX:46862427
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.883+2325A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862427 | ||||||
chrX:46862427
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0148 | 3 | NA18955.hp1 NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.883+2325A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862427 | ||||||
chrX:46862435
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883+2333C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862435 | ||||||
chrX:46862436
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0206 | 2 | HG01123.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.883+2334A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862436 | ||||||
chrX:46862443
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0206 | 2 | HG01123.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.883+2341A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862443 | ||||||
chrX:46862457
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.883+2355A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862457 | ||||||
chrX:46862471
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.883+2369T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862471 | ||||||
chrX:46862510
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(72): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.883+2408A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862510 | ||||||
chrX:46862516
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0039others(5): Show | 9 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.883+2414C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862516 | ||||||
chrX:46862553
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.883+2451A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862553 | ||||||
chrX:46862576
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.883+2474C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862576 | ||||||
chrX:46862591
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0130a0001c0001t0001g0131 | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+2489T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862591 | ||||||
chrX:46862593
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.883+2491G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862593 | ||||||
chrX:46862616
|
C | T | 3 | a0001c0001t0003g0010a0001c0001t0003g0037a0001c0001t0003g0038 | 4 | HG02622.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+2514C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862616 | ||||||
chrX:46862663
|
AAAAC | A | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.883+2581_883+2584d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46862663 | |||||
chrX:46862683
|
C | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.883+2581C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862683 | ||||||
chrX:46862905
|
G | C | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.883+2803G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862905 | ||||||
chrX:46863031
|
A | C | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+2929A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863031 | ||||||
chrX:46863046
|
A | T | 1 | a0001c0001t0004g0035 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+2944A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863046 | ||||||
chrX:46863083
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.883+2981T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863083 | ||||||
chrX:46863291
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883+3189A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863291 | ||||||
chrX:46863358
|
G | T | 1 | a0001c0001t0006g0211 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.883+3256G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863358 | ||||||
chrX:46863411
|
T | C | 1 | a0001c0001t0004g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883+3309T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863411 | ||||||
chrX:46863460
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.883+3358C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863460 | ||||||
chrX:46863832
|
T | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0061 | 5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+3730T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863832 | ||||||
chrX:46863950
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0155 | 2 | NA19001.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.883+3848C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863950 | ||||||
chrX:46864047
|
C | A | 1 | a0002c0002t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.883+3945C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864047 | ||||||
chrX:46864290
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.883+4188G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864290 | ||||||
chrX:46864347
|
C | CT | 26 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(23): Show | 28 | HG01081.hp2 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.883+4262dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | |||||
chrX:46864347
|
C | CTT | 6 | a0001c0001t0001g0042a0001c0001t0001g0177a0001c0001t0001g0220others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+4261_883+4262d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | |||||
chrX:46864347
|
CT | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0068others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+4262delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | |||||
chrX:46864411
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 9 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+4309A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864411 | ||||||
chrX:46864657
|
C | T | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158 | 3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.883+4555C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864657 | ||||||
chrX:46864674
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(87): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.883+4572G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864674 | ||||||
chrX:46864733
|
A | AC | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+4635dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864733 | |||||
chrX:46864832
|
AG | A | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+4733delG | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864832 | |||||
chrX:46865229
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.883+5127A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865229 | ||||||
chrX:46865478
|
G | C | 1 | a0001c0001t0003g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.883+5376G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865478 | ||||||
chrX:46865634
|
GAA | G | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.883+5534_883+5535d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46865634 | |||||
chrX:46865704
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.883+5602C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865704 | ||||||
chrX:46865925
|
C | CA | 2 | a0001c0001t0001g0118a0001c0001t0006g0212 | 2 | HG02071.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.883+5837dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46865925 | |||||
chrX:46866017
|
A | G | 1 | a0001c0003t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.883+5915A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866017 | ||||||
chrX:46866203
|
G | A | 2 | a0001c0001t0001g0025a0003c0004t0001g0025 | 2 | NA18971.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.883+6101G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866203 | ||||||
chrX:46866366
|
G | GTATC | 13 | a0001c0001t0001g0119a0001c0001t0002g0134a0001c0001t0002g0135others(10): Show | 14 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.883+6280_883+6283d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46866366 | |||||
chrX:46866367
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0004g0033 | 3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.883+6265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866367 | ||||||
chrX:46866382
|
C | CTAT | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+6283_883+6285d others(5): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46866382 | |||||
chrX:46866534
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+6432A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866534 | ||||||
chrX:46867131
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.883+7029C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867131 | ||||||
chrX:46867321
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.883+7219G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867321 | ||||||
chrX:46867538
|
G | GT | 2 | a0001c0001t0006g0211a0001c0001t0006g0212 | 2 | HG00558.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.883+7443dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46867538 | |||||
chrX:46867586
|
AT | A | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+7489delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46867586 | |||||
chrX:46867616
|
A | AT | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+7517dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46867616 | |||||
chrX:46867643
|
T | TC | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+7548dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46867643 | |||||
chrX:46867828
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.883+7726G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867828 | ||||||
chrX:46868049
|
AT | A | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883+7952delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868049 | |||||
chrX:46868051
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+7949T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868051 | ||||||
chrX:46868151
|
TC | T | 1 | a0001c0001t0001g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.883+8051delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868151 | |||||
chrX:46868309
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+8207G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868309 | ||||||
chrX:46868367
|
G | GA | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.883+8275dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868367 | |||||
chrX:46868583
|
G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0080others(17): Show | 24 | HG00558.hp2 HG00621.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.883+8481G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868583 | ||||||
chrX:46868743
|
GC | G | 1 | a0001c0001t0001g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.883+8643delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868743 | |||||
chrX:46868785
|
C | CA | 9 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0102others(6): Show | 9 | HG02055.hp1 HG02071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.883+8701dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868785 | |||||
chrX:46868785
|
CA | C | 2 | a0001c0001t0001g0031a0001c0001t0006g0211 | 2 | HG00558.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.883+8701delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868785 | |||||
chrX:46868838
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-8667G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868838 | ||||||
chrX:46869075
|
G | T | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-8430G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869075 | ||||||
chrX:46869300
|
CT | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(130): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.884-8190delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46869300 | |||||
chrX:46869578
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0130a0001c0001t0001g0131 | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-7927G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869578 | ||||||
chrX:46869591
|
A | T | 1 | a0001c0001t0006g0212 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.884-7914A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869591 | ||||||
chrX:46869606
|
C | CT | 14 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0093others(11): Show | 14 | HG01192.hp1 HG01981.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.884-7879dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46869606 | |||||
chrX:46869606
|
CT | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0200 | 2 | HG02897.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.884-7879delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46869606 | |||||
chrX:46869703
|
G | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-7802G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869703 | ||||||
chrX:46869704
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-7801G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869704 | ||||||
chrX:46869743
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.884-7762G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869743 | ||||||
chrX:46870140
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.884-7365C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870140 | ||||||
chrX:46870253
|
T | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-7252T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870253 | ||||||
chrX:46870273
|
A | AT | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.884-7222dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46870273 | |||||
chrX:46870273
|
AT | A | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.884-7222delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46870273 | |||||
chrX:46870674
|
A | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-6831A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870674 | ||||||
chrX:46870789
|
G | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0061 | 5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-6716G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870789 | ||||||
chrX:46870868
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0004g0033 | 3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.884-6637T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870868 | ||||||
chrX:46871009
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.884-6496C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871009 | ||||||
chrX:46871021
|
C | CT | 44 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0043others(41): Show | 46 | HG00438.hp1 HG00558.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.884-6458dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | |||||
chrX:46871021
|
C | CTT | 4 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.884-6459_884-6458d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | |||||
chrX:46871021
|
CT | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0079others(5): Show | 8 | HG00140.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-6458delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | |||||
chrX:46871021
|
CTT | C | 1 | a0001c0001t0005g0028 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.884-6459_884-6458d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | |||||
chrX:46871115
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-6390G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871115 | ||||||
chrX:46871146
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.884-6359C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871146 | ||||||
chrX:46871268
|
C | T | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-6237C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871268 | ||||||
chrX:46871513
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.884-5992G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871513 | ||||||
chrX:46871797
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.884-5708G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871797 | ||||||
chrX:46871949
|
AT | A | 1 | a0001c0001t0001g0041 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.884-5549delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871949 | |||||
chrX:46872014
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0166a0001c0001t0001g0167others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.884-5491C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872014 | ||||||
chrX:46872240
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.884-5265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872240 | ||||||
chrX:46872476
|
A | G | 1 | a0001c0001t0001g0021 | 2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.884-5029A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872476 | ||||||
chrX:46872722
|
T | TTTTG | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.884-4765_884-4762d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46872722 | |||||
chrX:46872773
|
T | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG00438.hp1 NA18973.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-4732T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872773 | ||||||
chrX:46872862
|
C | T | 1 | a0002c0002t0001g0123 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.884-4643C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872862 | ||||||
chrX:46873114
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-4391G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873114 | ||||||
chrX:46873279
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.884-4226T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873279 | ||||||
chrX:46873541
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.884-3964A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873541 | ||||||
chrX:46873556
|
GTTTTTT | G | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.884-3947_884-3942d others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46873556 | |||||
chrX:46873653
|
TA | T | 1 | a0001c0001t0007g0090 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.884-3849delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46873653 | |||||
chrX:46873988
|
A | AC | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.884-3513dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46873988 | |||||
chrX:46874557
|
T | TA | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.884-2938dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46874557 | |||||
chrX:46874825
|
G | GT | 1 | a0001c0001t0001g0121 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.884-2668dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46874825 | |||||
chrX:46874825
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.884-2680G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46874825 | ||||||
chrX:46874825
|
GT | G | 1 | a0005c0006t0001g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.884-2668delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46874825 | |||||
chrX:46874912
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.884-2593G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46874912 | ||||||
chrX:46875044
|
A | AT | 1 | a0001c0001t0003g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.884-2453dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875044 | |||||
chrX:46875044
|
AT | A | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.884-2453delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875044 | |||||
chrX:46875295
|
C | CT | 18 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 19 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.884-2195dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875295 | |||||
chrX:46875295
|
CT | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0130a0001c0001t0001g0199others(2): Show | 5 | HG02735.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-2195delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875295 | |||||
chrX:46875387
|
G | A | 1 | a0001c0001t0011g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.884-2118G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875387 | ||||||
chrX:46875640
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.884-1865G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875640 | ||||||
chrX:46875693
|
T | TCTCCTTT others(17): Show |
1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.884-1810_884-1787d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875693 | |||||
chrX:46875969
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.884-1536T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875969 | ||||||
chrX:46876016
|
A | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(88): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-1489A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876016 | ||||||
chrX:46876055
|
C | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-1450C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876055 | ||||||
chrX:46876116
|
A | AC | 1 | a0001c0001t0001g0104 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.884-1385dupC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46876116 | |||||
chrX:46876127
|
AT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(88): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-1368delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46876127 | |||||
chrX:46876162
|
C | T | 1 | a0001c0001t0004g0217 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.884-1343C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876162 | ||||||
chrX:46876418
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-1087G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876418 | ||||||
chrX:46876736
|
TTC | T | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.884-768_884-767del others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876736 | ||||||
chrX:46876770
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.884-735G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876770 | ||||||
chrX:46877020
|
T | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-485T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877020 | ||||||
chrX:46877283
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884-222A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877283 | ||||||
chrX:46877405
|
CA | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.884-97delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46877405 | |||||
chrX:46877461
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.884-44A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877461 | ||||||
chrX:46877650
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.969+60C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46877650 | ||||||
chrX:46877703
|
G | GGT | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(102): Show | 128 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.969+142_969+143dup others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877703
|
G | GGTGT | 7 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0188others(4): Show | 7 | HG00099.hp2 HG00544.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.969+140_969+143dup others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877703
|
G | GGTGTGT | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 115 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.969+138_969+143dup others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877703
|
G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0129others(1): Show | 6 | HG01069.hp1 HG01071.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+136_969+143dup others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877703
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.969+134_969+143dup others(10): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877703
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+128_969+143dup others(16): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | |||||
chrX:46877733
|
T | TGTG | 1 | a0001c0001t0001g0199 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.969+143_969+144ins others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46877733 | ||||||
chrX:46877734
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.969+144T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46877734 | ||||||
chrX:46878004
|
A | AT | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+419dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878004 | |||||
chrX:46878051
|
CA | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+466delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878051 | |||||
chrX:46878091
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T | C | 4 | a0001c0001t0003g0010a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+501T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878091 | ||||||
chrX:46878132
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T | TG | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+545dupG | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878132 | |||||
chrX:46878150
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G | A | 1 | a0001c0001t0001g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.969+560G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878150 | ||||||
chrX:46878237
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C | T | 1 | a0001c0001t0001g0059 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.969+647C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878237 | ||||||
chrX:46878240
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A | G | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.969+650A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878240 | ||||||
chrX:46878245
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C | T | 1 | a0001c0001t0001g0050 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.969+655C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878245 | ||||||
chrX:46878309
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G | A | 1 | a0001c0001t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.969+719G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878309 | ||||||
chrX:46878371
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T | C | 12 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.969+781T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878371 | ||||||
chrX:46878376
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C | CA | 12 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0067others(9): Show | 13 | HG01099.hp1 HG01891.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.969+802dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878376 | |||||
chrX:46878376
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CA | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+802delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878376 | |||||
chrX:46878836
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C | A | 1 | a0001c0001t0006g0212 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.970-850C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878836 | ||||||
chrX:46879061
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G | GT | 2 | a0001c0001t0001g0018a0001c0001t0001g0130 | 3 | HG02886.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.970-624dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879061 | |||||
chrX:46879062
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T | TA | 56 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(53): Show | 63 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.970-596dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | |||||
chrX:46879062
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T | TAA | 78 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 92 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.970-597_970-596dup others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | |||||
chrX:46879062
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T | TAAA | 22 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0075others(19): Show | 25 | HG00639.hp2 HG01081.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.970-598_970-596dup others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | |||||
chrX:46879062
|
T | TAAAA | 5 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0153others(2): Show | 6 | HG00642.hp1 HG01175.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-599_970-596dup others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | |||||
chrX:46879062
|
TA | T | 2 | a0001c0001t0001g0053a0001c0001t0002g0020 | 3 | HG02809.hp1 NA18945.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.970-596delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | |||||
chrX:46879311
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G | A | 1 | a0001c0001t0011g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.970-375G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879311 | ||||||
chrX:46879313
|
T | A | 1 | a0001c0003t0001g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.970-373T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879313 | ||||||
chrX:46879328
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GATT | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.970-350_970-348del others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879328 | |||||
chrX:46879538
|
TC | T | 1 | a0001c0001t0001g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.970-147delC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879538 | ||||||
chrX:46879572
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A | AG | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-114_970-113ins others(1): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879572 | ||||||
chrX:46879588
|
AATAATTA others(23): Show |
A | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-96_970-67delTA others(28): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879588 | |||||
chrX:46879621
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-65C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879621 | ||||||
chrX:46879624
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-62G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879624 | ||||||
chrX:46879633
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-53C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879633 | ||||||
chrX:46879634
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A | AC | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-52_970-51insC | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879634 | ||||||
chrX:46879655
|
A | ACTTT | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-31_970-30insCT others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879655 | ||||||
chrX:46879658
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T | A | 1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-28T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879658 |