geneid | 5746 |
---|---|
ensemblid | ENSG00000144407.10 |
hgncid | 9609 |
symbol | PTH2R |
name | parathyroid hormone 2 receptor |
refseq_nuc | NM_005048.4 |
refseq_prot | NP_005039.1 |
ensembl_nuc | ENST00000272847.7 |
ensembl_prot | ENSP00000272847.2 |
mane_status | MANE Select |
chr | chr2 |
start | 208406792 |
end | 208494506 |
strand | + |
ver | v1.2 |
region | chr2:208406792-208494506 |
region5000 | chr2:208401792-208499506 |
regionname0 | PTH2R_chr2_208406792_208494506 |
regionname5000 | PTH2R_chr2_208401792_208499506 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 550 | 281 | 79 | 30 | 126 | 11 | 33 | 92 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0002 | 0/0 | 550 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0003 | 0/0 | 550 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0004 | 0/0 | 550 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0005 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0006 | 0/0 | 81 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0007 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1653 | 149 | 29 | 17 | 76 | 7 | 19 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0002 | 1/0 | 1653 | 84 | 15 | 6 | 47 | 2 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0003 | 0/0 | 1653 | 42 | 30 | 7 | 2 | 2 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0004 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0005 | 0/0 | 1653 | 3 | 0 | 2 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0007 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0008 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0009 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0010 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0011 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0012 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
c0013 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1101 | 126 | 19 | 15 | 69 | 6 | 16 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0002 | 1/0 | 1100 | 87 | 14 | 8 | 48 | 3 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0003 | 0/0 | 1100 | 67 | 39 | 9 | 10 | 3 | 6 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0004 | 0/0 | 1100 | 6 | 6 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0005 | 0/0 | 1100 | 3 | 3 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0006 | 0/0 | 1100 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0007 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0008 | 0/0 | 1100 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0009 | 0/0 | 1100 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
t0010 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1653 | 149 | 29 | 17 | 76 | 7 | 19 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0002 | 1/0 | 1653 | 84 | 15 | 6 | 47 | 2 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0003 | 0/0 | 1653 | 42 | 30 | 7 | 2 | 2 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0006 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0008 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0010 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0011 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0002c0004 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0003c0005 | 0/0 | 1653 | 3 | 0 | 2 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0004c0007 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0005c0013 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0006c0009 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0007c0012 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2753 | 121 | 18 | 15 | 67 | 6 | 14 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0001t0003 | 0/0 | 2752 | 23 | 8 | 2 | 8 | 1 | 4 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0001t0005 | 0/0 | 2752 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0001t0006 | 0/0 | 2752 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0001t0007 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0001t0010 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0002t0002 | 1/0 | 2752 | 83 | 14 | 6 | 47 | 2 | 13 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0002t0008 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0003t0003 | 0/0 | 2752 | 41 | 29 | 7 | 2 | 2 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0003t0009 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0006t0001 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0006t0005 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0008t0003 | 0/0 | 2752 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0010t0002 | 0/0 | 2752 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0001c0011t0004 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0002c0004t0004 | 0/0 | 2752 | 5 | 5 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0003c0005t0002 | 0/0 | 2752 | 3 | 0 | 2 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0004c0007t0001 | 0/0 | 2753 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0005c0013t0001 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0006c0009t0001 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
a0007c0012t0003 | 0/0 | 2752 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | copy fasta | chr2 | 208401792 | 208499506 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0002t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0003t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0006t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0008t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0008t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0010t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0001c0011t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0002c0004t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0002c0004t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0002c0004t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0002c0004t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0002c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0003c0005t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0003c0005t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0003c0005t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0004c0007t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0005c0013t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0006c0009t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
a0007c0012t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0057 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0047 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0264 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | CHS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00735 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0010 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01106 | hp2 | a0001 | c0003 | t0003 | g0267 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0269 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01255 | hp1 | a0003 | c0005 | t0002 | g0056 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01261 | hp1 | a0001 | c0003 | t0003 | g0270 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01261 | hp2 | a0003 | c0005 | t0002 | g0055 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01433 | hp2 | a0001 | c0003 | t0003 | g0034 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01516 | hp2 | a0001 | c0003 | t0003 | g0266 | EUR | IBS | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01884 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0263 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02145 | hp2 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0259 | EAS | CDX | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02257 | hp1 | a0001 | c0003 | t0003 | g0155 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02258 | hp1 | a0001 | c0006 | t0005 | g0144 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02258 | hp2 | a0001 | c0003 | t0003 | g0143 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0153 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02451 | hp1 | a0001 | c0008 | t0003 | g0147 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0205 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02622 | hp2 | a0001 | c0003 | t0003 | g0031 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02630 | hp2 | a0001 | c0003 | t0003 | g0150 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02647 | hp2 | a0001 | c0003 | t0003 | g0039 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02717 | hp1 | a0001 | c0006 | t0001 | g0040 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0222 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02809 | hp1 | a0002 | c0004 | t0004 | g0272 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02886 | hp1 | a0001 | c0003 | t0003 | g0024 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02886 | hp2 | a0001 | c0003 | t0003 | g0169 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02895 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02896 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02896 | hp2 | a0002 | c0004 | t0004 | g0273 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0022 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0148 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02965 | hp1 | a0001 | c0003 | t0003 | g0029 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02976 | hp1 | a0001 | c0011 | t0004 | g0258 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03098 | hp1 | a0002 | c0004 | t0004 | g0274 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03098 | hp2 | a0001 | c0003 | t0003 | g0152 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03139 | hp1 | a0001 | c0003 | t0009 | g0151 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0145 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0038 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03209 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03239 | hp1 | a0006 | c0009 | t0001 | g0224 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03516 | hp2 | a0001 | c0003 | t0003 | g0156 | AFR | ESN | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0247 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0087 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0096 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03834 | hp2 | a0007 | c0012 | t0003 | g0163 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03927 | hp1 | a0005 | c0013 | t0001 | g0250 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0106 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0060 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04115 | hp2 | a0001 | c0003 | t0003 | g0149 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0067 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0154 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | CHB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | CHB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18952 | hp2 | a0004 | c0007 | t0001 | g0008 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18995 | hp1 | a0001 | c0010 | t0002 | g0255 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19001 | hp1 | a0004 | c0007 | t0001 | g0008 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19030 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19091 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19240 | hp1 | a0002 | c0004 | t0004 | g0268 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0045 | AFR | YRI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20752 | hp1 | a0003 | c0005 | t0002 | g0121 | EUR | TSI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0158 | EUR | TSI | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | GIH | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02109 | hp2 | a0001 | c0003 | t0003 | g0033 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02486 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03471 | hp1 | a0002 | c0004 | t0004 | g0271 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
HG03471 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | MSL | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
NA21309 | hp2 | a0001 | c0008 | t0003 | g0146 | AFR | LWK | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0037 | REF | REF | PTH2R_chr2_208401792_208499506 | PTH2R | chr2 | 208401792 | 208499506 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:208407092
|
G | T | 1 | a0005 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.49G>T | p.Gly17Cys | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 301/2752 | 49/1653 | 17/550 | chr2 | 208407092 | ||
chr2:208437603
|
C | A | 1 | a0006 | 1 | HG03239.hp1 | stop_gained | HIGH | c.245C>A | p.Ser82* | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 3/13 | 497/2752 | 245/1653 | 82/550 | chr2 | 208437603 | ||
chr2:208442379
|
C | T | 1 | a0003 | 3 | HG01255.hp1 HG01261.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.427C>T | p.Arg143Cys | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/13 | 679/2752 | 427/1653 | 143/550 | chr2 | 208442379 | ||
chr2:208443511
|
G | T | 1 | a0007 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.673G>T | p.Ala225Ser | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/13 | 925/2752 | 673/1653 | 225/550 | chr2 | 208443511 | ||
chr2:208481137
|
T | C | 1 | a0004 | 2 | NA18952.hp2 NA19001.hp1 |
missense_variant | MODERATE | c.1049T>C | p.Val350Ala | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/13 | 1301/2752 | 1049/1653 | 350/550 | chr2 | 208481137 | ||
chr2:208493309
|
G | A | 1 | a0002 | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.1303G>A | p.Val435Met | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 1555/2752 | 1303/1653 | 435/550 | chr2 | 208493309 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:208442396
|
T | C | 1 | a0001c0010 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.444T>C | p.Tyr148Tyr | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/13 | 696/2752 | 444/1653 | 148/550 | chr2 | 208442396 | ||
chr2:208444736
|
C | T | 1 | a0001c0008 | 2 | HG02451.hp1 NA21309.hp2 |
splice_region_variant&synonymous_variant | LOW | c.702C>T | p.Ile234Ile | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/13 | 954/2752 | 702/1653 | 234/550 | chr2 | 208444736 | ||
chr2:208459943
|
G | A | 1 | a0001c0006 | 2 | HG02258.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.963G>A | p.Pro321Pro | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/13 | 1215/2752 | 963/1653 | 321/550 | chr2 | 208459943 | ||
chr2:208489072
|
C | T | 1 | a0001c0011 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1137C>T | p.Phe379Phe | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/13 | 1389/2752 | 1137/1653 | 379/550 | chr2 | 208489072 | ||
chr2:208489075
|
A | G | 2 | a0001c0003a0001c0008 | 44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
synonymous_variant | LOW | c.1140A>G | p.Val380Val | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/13 | 1392/2752 | 1140/1653 | 380/550 | chr2 | 208489075 | ||
chr2:208493302
|
C | T | 10 | a0001c0001a0001c0003a0001c0006others(7): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
synonymous_variant | LOW | c.1296C>T | p.Asn432Asn | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 1548/2752 | 1296/1653 | 432/550 | chr2 | 208493302 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:208406841
|
C | T | 1 | a0001c0001t0010 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 203 | chr2 | 208406841 | |||||
chr2:208406995
|
C | T | 1 | a0001c0003t0009 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/13 | 49 | chr2 | 208406995 | |||||
chr2:208493690
|
G | C | 2 | a0001c0011t0004a0002c0004t0004 | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 31 | chr2 | 208493690 | |||||
chr2:208493691
|
G | T | 2 | a0001c0011t0004a0002c0004t0004 | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*32G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 32 | chr2 | 208493691 | |||||
chr2:208493884
|
C | G | 1 | a0001c0002t0008 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 225 | chr2 | 208493884 | |||||
chr2:208493920
|
A | AT | 7 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(4): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*268dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 269 | INFO_REALIGN_3_PRIME | chr2 | 208493920 | ||||
chr2:208494011
|
T | A | 2 | a0001c0001t0005a0001c0006t0005 | 3 | HG02258.hp1 HG02630.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*352T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 352 | chr2 | 208494011 | |||||
chr2:208494226
|
C | T | 7 | a0001c0001t0003a0001c0003t0003a0001c0003t0009others(4): Show | 74 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*567C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 567 | chr2 | 208494226 | |||||
chr2:208494337
|
T | C | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*678T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 678 | chr2 | 208494337 | |||||
chr2:208494437
|
T | G | 1 | a0001c0001t0007 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 13/13 | 778 | chr2 | 208494437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:208407566
|
G | T | 1 | a0001c0001t0003g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+448G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407566 | ||||||
chr2:208407814
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+696T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407814 | ||||||
chr2:208407835
|
T | C | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+717T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407835 | ||||||
chr2:208407870
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+752A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208407870 | ||||||
chr2:208408196
|
G | A | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+1078G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408196 | ||||||
chr2:208408534
|
GA | G | 17 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(14): Show | 18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+1426delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408534 | |||||
chr2:208408603
|
T | C | 1 | a0001c0003t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+1485T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408603 | ||||||
chr2:208408719
|
G | GGAAAGAG others(15): Show |
6 | a0001c0001t0001g0265a0001c0003t0003g0015a0001c0003t0003g0150others(3): Show | 7 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(22): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408719 | |||||
chr2:208408719
|
G | GGAAAGAG others(17): Show |
1 | a0001c0001t0003g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(24): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408719 | |||||
chr2:208408721
|
A | AAAGAGAG others(14): Show |
1 | a0001c0003t0003g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(21): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408721 | |||||
chr2:208408722
|
A | AAGAG | 25 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0120others(22): Show | 29 | HG00597.hp1 HG02148.hp2 HG02630.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+1618_75+1621dup others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(17): Show |
5 | a0001c0003t0003g0010a0001c0003t0003g0153a0001c0003t0003g0154others(2): Show | 6 | HG01069.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(24): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(19): Show |
10 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0003g0159others(7): Show | 10 | HG01175.hp1 HG01261.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(26): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(21): Show |
5 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(2): Show | 5 | HG02615.hp1 HG03017.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(28): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(23): Show |
7 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0172others(4): Show | 7 | HG01496.hp2 HG01884.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(30): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(25): Show |
4 | a0001c0001t0001g0174a0001c0001t0003g0175a0002c0004t0004g0272others(1): Show | 4 | HG02809.hp1 HG02896.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(32): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(27): Show |
1 | a0001c0001t0003g0176 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(34): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(29): Show |
2 | a0001c0001t0003g0177a0002c0004t0004g0274 | 2 | HG02080.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(36): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(20): Show |
1 | a0001c0001t0003g0178 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(27): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408722
|
A | AAGAGAGA others(22): Show |
1 | a0001c0001t0003g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408722 | |||||
chr2:208408724
|
G | GAGAGAGA others(13): Show |
14 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(11): Show | 14 | HG00280.hp1 HG01433.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408724 | |||||
chr2:208408724
|
G | GAGAGAGA others(15): Show |
1 | a0001c0001t0003g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(22): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408724 | |||||
chr2:208408726
|
G | GAGAGAGA others(11): Show |
7 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(4): Show | 7 | HG02486.hp1 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408726 | |||||
chr2:208408726
|
G | GAGAGAGA others(13): Show |
1 | a0001c0003t0003g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+1621_75+1622ins others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408726 | |||||
chr2:208408728
|
G | GAGAGAGA others(9): Show |
3 | a0001c0003t0003g0143a0001c0003t0003g0145a0001c0006t0005g0144 | 3 | HG02258.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(16): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408728 | |||||
chr2:208408732
|
G | GAGAGAGA others(5): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 6 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(12): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408732 | |||||
chr2:208408736
|
G | GAGAGAGA others(1): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017 | 4 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1621_75+1622ins others(8): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408736 | |||||
chr2:208408740
|
A | AAGAGAGA others(11): Show |
1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+1630_75+1647dup others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408740 | |||||
chr2:208408740
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.75+1622A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408740 | ||||||
chr2:208408742
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.75+1624G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408742 | ||||||
chr2:208408742
|
G | GAA | 81 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0073others(78): Show | 86 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.75+1625_75+1626ins others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408742 | |||||
chr2:208408742
|
G | GAGAA | 78 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0180others(75): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+1627_75+1628ins others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208408742 | |||||
chr2:208408744
|
G | A | 1 | a0001c0002t0002g0042 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.75+1626G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408744 | ||||||
chr2:208408746
|
G | A | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+1628G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408746 | ||||||
chr2:208408765
|
A | AGAGAGAG others(10): Show |
1 | a0001c0003t0003g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+1647_75+1648ins others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408765 | ||||||
chr2:208408766
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(5): Show | 10 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1648A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408766 | ||||||
chr2:208408768
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(5): Show | 10 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+1650T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408768 | ||||||
chr2:208408788
|
A | G | 6 | a0001c0003t0003g0015a0001c0003t0003g0264a0001c0003t0003g0266others(3): Show | 7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1670A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408788 | ||||||
chr2:208408907
|
T | C | 33 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(30): Show | 34 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.75+1789T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408907 | ||||||
chr2:208408969
|
C | T | 3 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149 | 3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.75+1851C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208408969 | ||||||
chr2:208409048
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+1930G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409048 | ||||||
chr2:208409058
|
A | G | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+1940A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409058 | ||||||
chr2:208409094
|
C | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.75+1976C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409094 | ||||||
chr2:208409104
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.75+1986C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409104 | ||||||
chr2:208409126
|
T | C | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+2008T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409126 | ||||||
chr2:208409264
|
A | G | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+2146A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409264 | ||||||
chr2:208409306
|
A | G | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+2188A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409306 | ||||||
chr2:208409314
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0005g0142 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+2196T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409314 | ||||||
chr2:208409500
|
G | A | 1 | a0001c0003t0003g0259 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.75+2382G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409500 | ||||||
chr2:208409542
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.75+2424T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409542 | ||||||
chr2:208409550
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+2432A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409550 | ||||||
chr2:208409786
|
A | C | 1 | a0001c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.75+2668A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409786 | ||||||
chr2:208409834
|
A | G | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+2716A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409834 | ||||||
chr2:208409975
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.75+2857C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208409975 | ||||||
chr2:208410074
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(185): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.75+2956C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410074 | ||||||
chr2:208410149
|
G | A | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+3031G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410149 | ||||||
chr2:208410245
|
C | T | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.75+3127C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410245 | ||||||
chr2:208410314
|
A | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3196A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410314 | ||||||
chr2:208410451
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+3333T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410451 | ||||||
chr2:208410684
|
A | T | 1 | a0001c0001t0003g0162 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.75+3566A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410684 | ||||||
chr2:208410746
|
A | T | 1 | a0001c0001t0003g0162 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.75+3628A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208410746 | ||||||
chr2:208410762
|
T | TTG | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(22): Show | 28 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+3662_75+3663dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208410762 | |||||
chr2:208411067
|
G | A | 1 | a0001c0002t0002g0044 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.75+3949G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411067 | ||||||
chr2:208411323
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.75+4205T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411323 | ||||||
chr2:208411334
|
GA | G | 10 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(7): Show | 10 | HG02080.hp2 HG02523.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+4217delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411334 | ||||||
chr2:208411428
|
G | A | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.75+4310G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411428 | ||||||
chr2:208411579
|
G | A | 32 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(29): Show | 33 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.75+4461G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411579 | ||||||
chr2:208411752
|
T | C | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+4634T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411752 | ||||||
chr2:208411898
|
G | T | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.75+4780G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208411898 | ||||||
chr2:208412116
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.75+4998T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412116 | ||||||
chr2:208412390
|
A | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+5272A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412390 | ||||||
chr2:208412713
|
T | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+5595T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412713 | ||||||
chr2:208412743
|
A | T | 1 | a0001c0002t0002g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+5625A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412743 | ||||||
chr2:208412754
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.75+5636A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412754 | ||||||
chr2:208412867
|
G | A | 2 | a0001c0003t0003g0034a0001c0003t0003g0149 | 2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.75+5749G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208412867 | ||||||
chr2:208413014
|
T | C | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+5896T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413014 | ||||||
chr2:208413141
|
C | CCA | 12 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(9): Show | 12 | HG01099.hp1 HG01943.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+6052_75+6053dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
C | CCACA | 29 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(26): Show | 29 | HG01433.hp2 HG01884.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.75+6050_75+6053dup others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
C | CCACACA | 7 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(4): Show | 7 | HG02572.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+6048_75+6053dup others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
C | CCACACAC others(3): Show |
1 | a0001c0003t0003g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+6044_75+6053dup others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
C | CCACACAC others(5): Show |
1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+6042_75+6053dup others(12): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
CCA | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 13 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+6052_75+6053del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413141
|
CCACA | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(174): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.75+6050_75+6053del others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208413141 | |||||
chr2:208413172
|
G | C | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+6054G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413172 | ||||||
chr2:208413200
|
G | A | 1 | a0001c0002t0002g0049 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.75+6082G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413200 | ||||||
chr2:208413320
|
C | A | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+6202C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413320 | ||||||
chr2:208413331
|
A | G | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.75+6213A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413331 | ||||||
chr2:208413998
|
C | T | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.75+6880C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208413998 | ||||||
chr2:208414288
|
A | G | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.75+7170A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414288 | ||||||
chr2:208414545
|
T | C | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+7427T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414545 | ||||||
chr2:208414547
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+7429G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414547 | ||||||
chr2:208414862
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.75+7744C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208414862 | ||||||
chr2:208415072
|
G | A | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.75+7954G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415072 | ||||||
chr2:208415076
|
G | A | 1 | a0001c0002t0002g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.75+7958G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415076 | ||||||
chr2:208415104
|
A | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0173 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.75+7986A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415104 | ||||||
chr2:208415148
|
T | C | 1 | a0001c0002t0002g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.75+8030T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415148 | ||||||
chr2:208415204
|
T | C | 8 | a0001c0003t0003g0148a0001c0003t0003g0152a0001c0003t0003g0154others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+8086T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415204 | ||||||
chr2:208415374
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0005g0142 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+8256T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415374 | ||||||
chr2:208415428
|
G | A | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+8310G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415428 | ||||||
chr2:208415655
|
C | A | 1 | a0001c0003t0003g0026 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.75+8537C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415655 | ||||||
chr2:208415831
|
C | G | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+8713C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415831 | ||||||
chr2:208415836
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+8718G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415836 | ||||||
chr2:208415978
|
A | T | 1 | a0005c0013t0001g0250 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.75+8860A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208415978 | ||||||
chr2:208416066
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.75+8948C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416066 | ||||||
chr2:208416091
|
G | C | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+8973G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416091 | ||||||
chr2:208416132
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+9014G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416132 | ||||||
chr2:208416155
|
G | T | 26 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(23): Show | 26 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.75+9037G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416155 | ||||||
chr2:208416206
|
T | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+9088T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416206 | ||||||
chr2:208416343
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(3): Show | 8 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+9225T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416343 | ||||||
chr2:208416363
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.75+9245C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416363 | ||||||
chr2:208416460
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.75+9342C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416460 | ||||||
chr2:208416703
|
G | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(39): Show | 49 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+9585G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416703 | ||||||
chr2:208416790
|
T | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+9672T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416790 | ||||||
chr2:208416962
|
C | T | 12 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(9): Show | 12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+9844C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416962 | ||||||
chr2:208416981
|
C | T | 6 | a0001c0003t0003g0015a0001c0003t0003g0264a0001c0003t0003g0266others(3): Show | 7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9863C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208416981 | ||||||
chr2:208417075
|
T | C | 1 | a0001c0002t0002g0052 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+9957T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417075 | ||||||
chr2:208417233
|
C | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.75+10115C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417233 | ||||||
chr2:208417234
|
G | A | 3 | a0001c0003t0003g0148a0001c0003t0003g0152a0001c0011t0004g0258 | 3 | HG02922.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.75+10116G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417234 | ||||||
chr2:208417541
|
C | CT | 9 | a0001c0001t0001g0113a0001c0001t0001g0138a0001c0002t0002g0099others(6): Show | 9 | HG00597.hp1 HG01175.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+10452dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417541
|
CT | C | 127 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(124): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.75+10452delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417541
|
CTT | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG01255.hp2 HG01993.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+10451_75+10452d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417541
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.75+10442_75+10452d others(13): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417541
|
CTTTTTTT others(8): Show |
C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+10438_75+10452d others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417541
|
CTTTTTTT others(9): Show |
C | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(44): Show | 49 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+10437_75+10452d others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208417541 | |||||
chr2:208417572
|
T | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.75+10454T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417572 | ||||||
chr2:208417651
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+10533G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417651 | ||||||
chr2:208417731
|
A | G | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-10470A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417731 | ||||||
chr2:208417963
|
C | A | 7 | a0001c0003t0003g0148a0001c0003t0003g0152a0001c0003t0003g0154others(4): Show | 7 | HG02257.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-10238C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208417963 | ||||||
chr2:208418282
|
C | T | 1 | a0001c0002t0002g0189 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.76-9919C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418282 | ||||||
chr2:208418363
|
A | AT | 17 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(14): Show | 18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-9827dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208418363 | |||||
chr2:208418363
|
AT | A | 41 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(38): Show | 41 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(38): Show |
intron_variant | MODIFIER | c.76-9827delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208418363 | |||||
chr2:208418377
|
G | A | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.76-9824G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418377 | ||||||
chr2:208418529
|
C | T | 3 | a0001c0001t0003g0158a0001c0001t0003g0164a0007c0012t0003g0163 | 3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.76-9672C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418529 | ||||||
chr2:208418576
|
T | C | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.76-9625T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418576 | ||||||
chr2:208418623
|
C | A | 1 | a0001c0001t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.76-9578C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418623 | ||||||
chr2:208418667
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-9534G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418667 | ||||||
chr2:208418868
|
C | T | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-9333C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418868 | ||||||
chr2:208418884
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.76-9317A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208418884 | ||||||
chr2:208419391
|
T | G | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-8810T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419391 | ||||||
chr2:208419457
|
C | T | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-8744C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419457 | ||||||
chr2:208419792
|
T | C | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-8409T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208419792 | ||||||
chr2:208420210
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.76-7991C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420210 | ||||||
chr2:208420441
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.76-7760G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420441 | ||||||
chr2:208420534
|
ATTAAC | A | 12 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(9): Show | 13 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-7662_76-7658del others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208420534 | |||||
chr2:208420655
|
G | A | 5 | a0001c0001t0003g0157a0001c0001t0003g0170a0001c0001t0003g0171others(2): Show | 5 | HG01496.hp2 HG01884.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-7546G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420655 | ||||||
chr2:208420707
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.76-7494A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420707 | ||||||
chr2:208420744
|
A | G | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-7457A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420744 | ||||||
chr2:208420781
|
T | G | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-7420T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420781 | ||||||
chr2:208420807
|
C | T | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-7394C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420807 | ||||||
chr2:208420983
|
C | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(39): Show | 49 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.76-7218C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208420983 | ||||||
chr2:208421016
|
C | T | 4 | a0001c0003t0003g0028a0001c0003t0003g0029a0001c0003t0003g0031others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-7185C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421016 | ||||||
chr2:208421049
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.76-7152T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421049 | ||||||
chr2:208421094
|
G | C | 69 | a0001c0001t0001g0073a0001c0001t0003g0095a0001c0002t0002g0006others(66): Show | 72 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-7107G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421094 | ||||||
chr2:208421240
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0005g0142 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-6961C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421240 | ||||||
chr2:208421365
|
G | GGT | 23 | a0001c0001t0001g0238a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-6815_76-6814dup others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208421365 | |||||
chr2:208421365
|
G | T | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.76-6836G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421365 | ||||||
chr2:208421417
|
G | T | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-6784G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421417 | ||||||
chr2:208421508
|
A | G | 61 | a0001c0001t0001g0073a0001c0001t0003g0095a0001c0002t0002g0006others(58): Show | 64 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.76-6693A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421508 | ||||||
chr2:208421601
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6600A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421601 | ||||||
chr2:208421895
|
C | T | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-6306C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208421895 | ||||||
chr2:208422082
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(184): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.76-6119C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422082 | ||||||
chr2:208422122
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.76-6079G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422122 | ||||||
chr2:208422202
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.76-5999A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422202 | ||||||
chr2:208422271
|
A | G | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5930A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422271 | ||||||
chr2:208422495
|
C | T | 8 | a0001c0003t0003g0148a0001c0003t0003g0152a0001c0003t0003g0154others(5): Show | 8 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-5706C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422495 | ||||||
chr2:208422516
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.76-5685G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422516 | ||||||
chr2:208422525
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.76-5676T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422525 | ||||||
chr2:208422601
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 5 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-5600C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422601 | ||||||
chr2:208422739
|
A | G | 1 | a0001c0002t0002g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.76-5462A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422739 | ||||||
chr2:208422883
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.76-5318G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422883 | ||||||
chr2:208422934
|
A | G | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-5267A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208422934 | ||||||
chr2:208423157
|
G | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.76-5044G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423157 | ||||||
chr2:208423167
|
G | A | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-5034G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423167 | ||||||
chr2:208423346
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(184): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.76-4855T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423346 | ||||||
chr2:208423348
|
G | A | 1 | a0001c0002t0002g0061 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.76-4853G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423348 | ||||||
chr2:208423477
|
C | G | 69 | a0001c0001t0001g0073a0001c0001t0003g0095a0001c0002t0002g0006others(66): Show | 72 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-4724C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423477 | ||||||
chr2:208423738
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 5 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4463A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423738 | ||||||
chr2:208423765
|
GCT | G | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.76-4433_76-4432del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208423765 | |||||
chr2:208423808
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0005g0142 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-4393T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423808 | ||||||
chr2:208423960
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(184): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.76-4241G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208423960 | ||||||
chr2:208424058
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(39): Show | 49 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.76-4143G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424058 | ||||||
chr2:208424080
|
G | A | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.76-4121G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424080 | ||||||
chr2:208424081
|
C | T | 1 | a0001c0002t0002g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-4120C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424081 | ||||||
chr2:208424090
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76-4111C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424090 | ||||||
chr2:208424470
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.76-3731C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424470 | ||||||
chr2:208424877
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(2): Show | 7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3324G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208424877 | ||||||
chr2:208425025
|
T | G | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.76-3176T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208425025 | ||||||
chr2:208425521
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.76-2680A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208425521 | ||||||
chr2:208426130
|
A | G | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.76-2071A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426130 | ||||||
chr2:208426210
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0003g0164 | 2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.76-1991C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426210 | ||||||
chr2:208426403
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.76-1798T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426403 | ||||||
chr2:208426420
|
T | C | 4 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064others(1): Show | 4 | HG00423.hp1 HG02071.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1781T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426420 | ||||||
chr2:208426591
|
A | G | 1 | a0002c0004t0004g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.76-1610A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426591 | ||||||
chr2:208426614
|
T | C | 1 | a0001c0003t0003g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.76-1587T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426614 | ||||||
chr2:208426639
|
A | G | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-1562A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426639 | ||||||
chr2:208426674
|
T | G | 1 | a0001c0003t0003g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-1527T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426674 | ||||||
chr2:208426703
|
C | T | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1498C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426703 | ||||||
chr2:208426719
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(186): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.76-1482G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426719 | ||||||
chr2:208426785
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(2): Show | 7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-1416A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426785 | ||||||
chr2:208426909
|
T | C | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-1292T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208426909 | ||||||
chr2:208427210
|
G | GA | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0018others(2): Show | 7 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-984dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 208427210 | |||||
chr2:208427230
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.76-971A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427230 | ||||||
chr2:208427233
|
C | T | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-968C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427233 | ||||||
chr2:208427318
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.76-883C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427318 | ||||||
chr2:208427468
|
A | G | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-733A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427468 | ||||||
chr2:208427542
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.76-659T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427542 | ||||||
chr2:208427599
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18940.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.76-602A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427599 | ||||||
chr2:208427628
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.76-573G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427628 | ||||||
chr2:208427649
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-552A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427649 | ||||||
chr2:208427723
|
A | C | 13 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(10): Show | 13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-478A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 1/12 | chr2 | 208427723 | ||||||
chr2:208428443
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(239): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.178+140C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428443 | ||||||
chr2:208428468
|
C | G | 6 | a0001c0001t0003g0157a0001c0001t0003g0165a0001c0001t0003g0170others(3): Show | 6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+165C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428468 | ||||||
chr2:208428556
|
C | G | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+253C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428556 | ||||||
chr2:208428574
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0005g0142 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+271G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428574 | ||||||
chr2:208428612
|
C | T | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.178+309C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428612 | ||||||
chr2:208428639
|
G | A | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.178+336G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428639 | ||||||
chr2:208428772
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178+469A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428772 | ||||||
chr2:208428813
|
G | A | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+510G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428813 | ||||||
chr2:208428862
|
A | G | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.178+559A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428862 | ||||||
chr2:208428951
|
G | A | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.178+648G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208428951 | ||||||
chr2:208429011
|
G | C | 4 | a0001c0003t0003g0038a0001c0003t0003g0039a0001c0003t0003g0148others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+708G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429011 | ||||||
chr2:208429025
|
C | T | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+722C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429025 | ||||||
chr2:208429026
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.178+723G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429026 | ||||||
chr2:208429039
|
C | T | 145 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(142): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.178+736C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429039 | ||||||
chr2:208429084
|
CA | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(160): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.178+799delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208429084 | |||||
chr2:208429084
|
CAA | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(96): Show | 107 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.178+798_178+799del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208429084 | |||||
chr2:208429229
|
G | C | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+926G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429229 | ||||||
chr2:208429252
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 58 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.178+949A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429252 | ||||||
chr2:208429307
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.178+1004C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429307 | ||||||
chr2:208429362
|
T | G | 1 | a0001c0001t0003g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.178+1059T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429362 | ||||||
chr2:208429440
|
T | C | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.178+1137T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429440 | ||||||
chr2:208429486
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+1183C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429486 | ||||||
chr2:208429572
|
T | C | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178+1269T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429572 | ||||||
chr2:208429652
|
A | T | 1 | a0001c0002t0002g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.178+1349A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429652 | ||||||
chr2:208429694
|
A | T | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.178+1391A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208429694 | ||||||
chr2:208430093
|
T | A | 31 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(28): Show | 32 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.178+1790T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430093 | ||||||
chr2:208430291
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178+1988A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430291 | ||||||
chr2:208430460
|
C | A | 1 | a0001c0002t0002g0065 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.178+2157C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430460 | ||||||
chr2:208430546
|
C | CT | 42 | a0001c0001t0001g0233a0001c0001t0001g0260a0001c0001t0001g0261others(39): Show | 43 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.178+2261dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208430546 | |||||
chr2:208430555
|
T | TC | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(44): Show | 56 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+2252_178+2253i others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430555 | ||||||
chr2:208430893
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0120a0001c0001t0001g0134others(1): Show | 5 | NA18942.hp1 NA18950.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+2590A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430893 | ||||||
chr2:208430911
|
T | C | 145 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(142): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.178+2608T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430911 | ||||||
chr2:208430981
|
T | C | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+2678T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208430981 | ||||||
chr2:208431004
|
C | T | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+2701C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431004 | ||||||
chr2:208431102
|
T | C | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178+2799T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431102 | ||||||
chr2:208431290
|
A | G | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.178+2987A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431290 | ||||||
chr2:208431345
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+3042A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431345 | ||||||
chr2:208431411
|
G | A | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+3108G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431411 | ||||||
chr2:208431702
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.178+3399A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431702 | ||||||
chr2:208431780
|
T | C | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.178+3477T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208431780 | ||||||
chr2:208432218
|
G | T | 67 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(64): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.178+3915G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432218 | ||||||
chr2:208432301
|
G | A | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+3998G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432301 | ||||||
chr2:208432532
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.178+4229T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432532 | ||||||
chr2:208432594
|
T | C | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+4291T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432594 | ||||||
chr2:208432615
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(40): Show | 51 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.178+4312C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432615 | ||||||
chr2:208432679
|
G | A | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.178+4376G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432679 | ||||||
chr2:208432941
|
G | A | 1 | a0001c0002t0002g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.179-4596G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432941 | ||||||
chr2:208432985
|
G | A | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-4552G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432985 | ||||||
chr2:208432992
|
G | A | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-4545G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208432992 | ||||||
chr2:208433078
|
G | C | 13 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(10): Show | 13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-4459G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433078 | ||||||
chr2:208433079
|
G | A | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-4458G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433079 | ||||||
chr2:208433106
|
A | T | 8 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(5): Show | 8 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-4431A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433106 | ||||||
chr2:208433305
|
T | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(40): Show | 50 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.179-4232T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433305 | ||||||
chr2:208433411
|
A | G | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-4126A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433411 | ||||||
chr2:208433688
|
C | T | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-3849C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433688 | ||||||
chr2:208433908
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(46): Show | 58 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.179-3629T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208433908 | ||||||
chr2:208434040
|
G | A | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.179-3497G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434040 | ||||||
chr2:208434095
|
C | T | 1 | a0001c0003t0003g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-3442C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434095 | ||||||
chr2:208434130
|
A | G | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.179-3407A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434130 | ||||||
chr2:208434214
|
T | C | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179-3323T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434214 | ||||||
chr2:208434299
|
C | CA | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0237others(5): Show | 8 | HG01884.hp2 HG02071.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-3225dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208434299 | |||||
chr2:208434390
|
A | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-3147A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434390 | ||||||
chr2:208434641
|
C | T | 4 | a0001c0003t0003g0028a0001c0003t0003g0029a0001c0003t0003g0031others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2896C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434641 | ||||||
chr2:208434706
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0245 | 2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.179-2831C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434706 | ||||||
chr2:208434744
|
T | G | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179-2793T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434744 | ||||||
chr2:208434805
|
A | T | 1 | a0001c0002t0002g0084 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.179-2732A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208434805 | ||||||
chr2:208435005
|
G | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0265 | 3 | HG01099.hp1 HG02015.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.179-2532G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435005 | ||||||
chr2:208435183
|
A | G | 1 | a0001c0003t0003g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179-2354A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435183 | ||||||
chr2:208435206
|
G | A | 1 | a0001c0002t0002g0094 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.179-2331G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435206 | ||||||
chr2:208435353
|
G | A | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-2184G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435353 | ||||||
chr2:208435410
|
G | A | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-2127G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435410 | ||||||
chr2:208435437
|
G | A | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-2100G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435437 | ||||||
chr2:208435546
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.179-1991A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435546 | ||||||
chr2:208435563
|
C | T | 3 | a0001c0001t0003g0158a0001c0001t0003g0164a0007c0012t0003g0163 | 3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.179-1974C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435563 | ||||||
chr2:208435721
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.179-1816C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435721 | ||||||
chr2:208435833
|
C | A | 1 | a0001c0002t0002g0066 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.179-1704C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435833 | ||||||
chr2:208435893
|
A | C | 1 | a0001c0001t0003g0167 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.179-1644A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208435893 | ||||||
chr2:208436052
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0190 | 3 | HG00423.hp2 HG00621.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.179-1485G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436052 | ||||||
chr2:208436066
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.179-1471C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436066 | ||||||
chr2:208436242
|
G | A | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.179-1295G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436242 | ||||||
chr2:208436288
|
AG | A | 147 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.179-1246delG | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 208436288 | |||||
chr2:208436480
|
A | G | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.179-1057A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436480 | ||||||
chr2:208436506
|
C | T | 3 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149 | 3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.179-1031C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436506 | ||||||
chr2:208436541
|
A | T | 1 | a0001c0001t0003g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.179-996A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436541 | ||||||
chr2:208436698
|
G | A | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.179-839G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436698 | ||||||
chr2:208436726
|
G | C | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-811G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436726 | ||||||
chr2:208436918
|
G | A | 1 | a0001c0001t0007g0187 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.179-619G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436918 | ||||||
chr2:208436920
|
C | T | 1 | a0002c0004t0004g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179-617C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436920 | ||||||
chr2:208436959
|
G | A | 13 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(10): Show | 13 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-578G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208436959 | ||||||
chr2:208437057
|
A | G | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 4 | HG01099.hp1 HG01943.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-480A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437057 | ||||||
chr2:208437062
|
T | C | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.179-475T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437062 | ||||||
chr2:208437194
|
A | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0231 | 2 | NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.179-343A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437194 | ||||||
chr2:208437381
|
T | A | 4 | a0001c0003t0003g0038a0001c0003t0003g0039a0001c0003t0003g0148others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-156T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437381 | ||||||
chr2:208437438
|
C | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.179-99C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 2/12 | chr2 | 208437438 | ||||||
chr2:208437748
|
A | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.290-12A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 3/12 | chr2 | 208437748 | ||||||
chr2:208438148
|
C | CA | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.411+267_411+268ins others(1): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438148 | ||||||
chr2:208438161
|
A | T | 1 | a0001c0002t0002g0194 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.411+280A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438161 | ||||||
chr2:208438265
|
G | A | 1 | a0001c0003t0003g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.411+384G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438265 | ||||||
chr2:208438646
|
A | G | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+765A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438646 | ||||||
chr2:208438657
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.411+776A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208438657 | ||||||
chr2:208439025
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0207a0001c0001t0001g0230others(1): Show | 4 | HG02027.hp1 HG02071.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1144A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439025 | ||||||
chr2:208439183
|
A | G | 17 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(14): Show | 18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.411+1302A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439183 | ||||||
chr2:208439511
|
A | G | 1 | a0001c0003t0003g0023 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.411+1630A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439511 | ||||||
chr2:208439533
|
A | G | 1 | a0001c0002t0002g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.411+1652A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439533 | ||||||
chr2:208439619
|
C | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.411+1738C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439619 | ||||||
chr2:208439722
|
G | T | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.411+1841G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439722 | ||||||
chr2:208439771
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.411+1890T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439771 | ||||||
chr2:208439941
|
A | G | 2 | a0001c0002t0002g0083a0001c0002t0002g0089 | 2 | NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.411+2060A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439941 | ||||||
chr2:208439992
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.411+2111C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208439992 | ||||||
chr2:208440165
|
C | T | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-2199C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440165 | ||||||
chr2:208440378
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017 | 4 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-1986T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440378 | ||||||
chr2:208440529
|
A | G | 1 | a0001c0001t0003g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412-1835A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440529 | ||||||
chr2:208440557
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0244 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.412-1807A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440557 | ||||||
chr2:208440689
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.412-1675A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440689 | ||||||
chr2:208440804
|
G | T | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-1560G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440804 | ||||||
chr2:208440960
|
C | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.412-1404C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208440960 | ||||||
chr2:208441082
|
AGCCAATT others(10): Show |
A | 1 | a0001c0002t0002g0066 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.412-1278_412-1262d others(19): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 208441082 | |||||
chr2:208441206
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.412-1158G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441206 | ||||||
chr2:208441230
|
A | G | 1 | a0001c0003t0003g0270 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-1134A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441230 | ||||||
chr2:208441253
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.412-1111C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441253 | ||||||
chr2:208441254
|
A | G | 17 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.412-1110A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441254 | ||||||
chr2:208441350
|
A | G | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.412-1014A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441350 | ||||||
chr2:208441479
|
G | A | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-885G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441479 | ||||||
chr2:208441603
|
T | C | 1 | a0002c0004t0004g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.412-761T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441603 | ||||||
chr2:208441671
|
G | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.412-693G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441671 | ||||||
chr2:208441768
|
T | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0245 | 2 | NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.412-596T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441768 | ||||||
chr2:208441854
|
G | A | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.412-510G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441854 | ||||||
chr2:208441981
|
C | T | 1 | a0005c0013t0001g0250 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.412-383C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208441981 | ||||||
chr2:208442068
|
G | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.412-296G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442068 | ||||||
chr2:208442096
|
C | T | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-268C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442096 | ||||||
chr2:208442201
|
T | C | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-163T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442201 | ||||||
chr2:208442204
|
A | G | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412-160A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442204 | ||||||
chr2:208442216
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.412-148C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 4/12 | chr2 | 208442216 | ||||||
chr2:208442729
|
G | A | 2 | a0001c0003t0003g0034a0001c0003t0003g0149 | 2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.509+268G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442729 | ||||||
chr2:208442814
|
A | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+353A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442814 | ||||||
chr2:208442988
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.510-360A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208442988 | ||||||
chr2:208443143
|
A | G | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.510-205A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443143 | ||||||
chr2:208443155
|
T | C | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-193T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443155 | ||||||
chr2:208443160
|
T | A | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-188T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 5/12 | chr2 | 208443160 | ||||||
chr2:208443762
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+225G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208443762 | ||||||
chr2:208443837
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019 | 4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+300C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208443837 | ||||||
chr2:208444056
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.699+519G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444056 | ||||||
chr2:208444405
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.700-329C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444405 | ||||||
chr2:208444672
|
A | C | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.700-62A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444672 | ||||||
chr2:208444721
|
T | G | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.700-13T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 6/12 | chr2 | 208444721 | ||||||
chr2:208444995
|
C | G | 2 | a0001c0003t0003g0145a0001c0006t0005g0144 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.853+108C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208444995 | ||||||
chr2:208445070
|
C | T | 17 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0160others(14): Show | 17 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.853+183C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445070 | ||||||
chr2:208445076
|
G | C | 1 | a0001c0002t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853+189G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445076 | ||||||
chr2:208445108
|
T | A | 17 | a0001c0003t0003g0010a0001c0003t0003g0021a0001c0003t0003g0022others(14): Show | 18 | HG01069.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.853+221T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445108 | ||||||
chr2:208445462
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(43): Show | 55 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.853+575C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445462 | ||||||
chr2:208445639
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.853+752C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445639 | ||||||
chr2:208445699
|
C | G | 1 | a0001c0001t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.853+812C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445699 | ||||||
chr2:208445939
|
A | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+1052A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208445939 | ||||||
chr2:208446154
|
A | G | 1 | a0001c0003t0003g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.853+1267A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446154 | ||||||
chr2:208446284
|
C | T | 13 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.853+1397C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446284 | ||||||
chr2:208446327
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.853+1440G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446327 | ||||||
chr2:208446455
|
G | A | 2 | a0001c0003t0003g0010a0001c0006t0001g0040 | 3 | HG01069.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.853+1568G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446455 | ||||||
chr2:208446499
|
T | C | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+1612T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446499 | ||||||
chr2:208446661
|
T | C | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+1774T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446661 | ||||||
chr2:208446867
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853+1980A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446867 | ||||||
chr2:208446916
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.853+2029C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208446916 | ||||||
chr2:208447257
|
C | T | 1 | a0001c0002t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853+2370C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447257 | ||||||
chr2:208447433
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.853+2546A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447433 | ||||||
chr2:208447449
|
G | A | 12 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(9): Show | 12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2562G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447449 | ||||||
chr2:208447491
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.853+2604A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447491 | ||||||
chr2:208447587
|
C | CA | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 78 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.853+2710dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447587 | |||||
chr2:208447587
|
CA | C | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0145others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.853+2710delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447587 | |||||
chr2:208447606
|
A | AAAAT | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(64): Show | 75 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.853+2754_853+2757d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | |||||
chr2:208447606
|
AAAAT | A | 164 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(161): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.853+2754_853+2757d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | |||||
chr2:208447606
|
AAAATAAA others(5): Show |
A | 4 | a0001c0003t0003g0038a0001c0003t0003g0039a0001c0003t0003g0148others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+2746_853+2757d others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208447606 | |||||
chr2:208447791
|
T | C | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.853+2904T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447791 | ||||||
chr2:208447913
|
T | C | 72 | a0001c0001t0001g0073a0001c0001t0001g0191a0001c0001t0001g0210others(69): Show | 75 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.854-2836T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208447913 | ||||||
chr2:208448046
|
C | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.854-2703C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448046 | ||||||
chr2:208448162
|
C | T | 17 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(14): Show | 18 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.854-2587C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448162 | ||||||
chr2:208448284
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.854-2465T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448284 | ||||||
chr2:208448315
|
T | A | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.854-2434T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448315 | ||||||
chr2:208448377
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.854-2372A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448377 | ||||||
chr2:208448566
|
G | A | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.854-2183G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448566 | ||||||
chr2:208448582
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.854-2167C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208448582 | ||||||
chr2:208449132
|
A | G | 1 | a0001c0003t0003g0010 | 2 | HG01069.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.854-1617A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449132 | ||||||
chr2:208449244
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.854-1505T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449244 | ||||||
chr2:208449300
|
G | A | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-1449G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449300 | ||||||
chr2:208449437
|
T | TGATA | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.854-1299_854-1296d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | |||||
chr2:208449437
|
T | TGATAGAT others(1): Show |
114 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(111): Show | 125 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.854-1303_854-1296d others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | |||||
chr2:208449437
|
T | TGATAGAT others(5): Show |
51 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0108others(48): Show | 53 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.854-1307_854-1296d others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | |||||
chr2:208449437
|
T | TGATAGAT others(9): Show |
5 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0233others(2): Show | 5 | HG00597.hp2 HG02027.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-1311_854-1296d others(18): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449437 | |||||
chr2:208449446
|
GATAGATA others(1): Show |
G | 3 | a0001c0001t0001g0141a0001c0001t0005g0140a0001c0001t0005g0142 | 3 | HG02486.hp2 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.854-1295_854-1288d others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449446 | |||||
chr2:208449450
|
GATAA | G | 3 | a0001c0001t0003g0158a0001c0001t0003g0167a0001c0003t0003g0169 | 3 | HG02886.hp2 HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.854-1295_854-1292d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 208449450 | |||||
chr2:208449454
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(264): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.854-1295A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449454 | ||||||
chr2:208449480
|
A | T | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.854-1269A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449480 | ||||||
chr2:208449800
|
A | C | 1 | a0001c0002t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.854-949A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449800 | ||||||
chr2:208449822
|
A | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.854-927A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208449822 | ||||||
chr2:208450132
|
T | C | 3 | a0001c0002t0002g0112a0001c0002t0002g0114a0001c0002t0002g0115 | 3 | HG02738.hp2 HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.854-617T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450132 | ||||||
chr2:208450185
|
T | C | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-564T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450185 | ||||||
chr2:208450211
|
A | C | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.854-538A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450211 | ||||||
chr2:208450296
|
A | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(42): Show | 53 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.854-453A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450296 | ||||||
chr2:208450370
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.854-379C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450370 | ||||||
chr2:208450397
|
A | C | 4 | a0001c0003t0003g0038a0001c0003t0003g0039a0001c0003t0003g0148others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-352A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450397 | ||||||
chr2:208450473
|
T | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.854-276T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450473 | ||||||
chr2:208450720
|
C | T | 1 | a0001c0002t0008g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.854-29C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450720 | ||||||
chr2:208450721
|
T | C | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-28T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450721 | ||||||
chr2:208450722
|
A | T | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-27A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450722 | ||||||
chr2:208450723
|
G | T | 15 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0148others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-26G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 7/12 | chr2 | 208450723 | ||||||
chr2:208450848
|
G | A | 146 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(143): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.914+39G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208450848 | ||||||
chr2:208451249
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(42): Show | 53 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.914+440C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451249 | ||||||
chr2:208451373
|
G | T | 4 | a0001c0003t0003g0038a0001c0003t0003g0039a0001c0003t0003g0148others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+564G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451373 | ||||||
chr2:208451571
|
T | C | 5 | a0001c0002t0002g0070a0001c0002t0002g0078a0001c0002t0002g0084others(2): Show | 5 | HG02083.hp1 NA18940.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+762T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451571 | ||||||
chr2:208451680
|
A | G | 1 | a0001c0003t0003g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.914+871A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451680 | ||||||
chr2:208451857
|
T | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019 | 4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+1048T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451857 | ||||||
chr2:208451995
|
C | T | 1 | a0001c0002t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1186C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208451995 | ||||||
chr2:208452035
|
A | G | 216 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(213): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.914+1226A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452035 | ||||||
chr2:208452468
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.914+1659C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452468 | ||||||
chr2:208452627
|
G | A | 1 | a0001c0003t0003g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914+1818G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452627 | ||||||
chr2:208452694
|
G | T | 1 | a0001c0002t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+1885G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452694 | ||||||
chr2:208452762
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.914+1953A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452762 | ||||||
chr2:208452847
|
G | C | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914+2038G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452847 | ||||||
chr2:208452857
|
G | A | 23 | a0001c0001t0001g0174a0001c0001t0003g0157a0001c0001t0003g0158others(20): Show | 23 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.914+2048G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452857 | ||||||
chr2:208452925
|
G | A | 1 | a0001c0003t0003g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.914+2116G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208452925 | ||||||
chr2:208453068
|
G | A | 148 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(145): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.914+2259G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453068 | ||||||
chr2:208453112
|
C | T | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+2303C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453112 | ||||||
chr2:208453153
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.914+2344C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453153 | ||||||
chr2:208453475
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.914+2666A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453475 | ||||||
chr2:208453609
|
G | T | 27 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0003g0157others(24): Show | 27 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.914+2800G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453609 | ||||||
chr2:208453661
|
A | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+2852A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453661 | ||||||
chr2:208453676
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.914+2867G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453676 | ||||||
chr2:208453718
|
A | G | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.914+2909A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453718 | ||||||
chr2:208453733
|
C | T | 46 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0003g0157others(43): Show | 46 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(43): Show |
intron_variant | MODIFIER | c.914+2924C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453733 | ||||||
chr2:208453769
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.914+2960A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453769 | ||||||
chr2:208453927
|
C | T | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+3118C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453927 | ||||||
chr2:208453934
|
T | A | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+3125T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208453934 | ||||||
chr2:208454165
|
CT | C | 6 | a0001c0003t0003g0039a0001c0003t0003g0169a0001c0006t0001g0040others(3): Show | 6 | HG01255.hp1 HG01261.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+3366delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208454165 | |||||
chr2:208454204
|
G | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG00609.hp1 NA18939.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+3395G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454204 | ||||||
chr2:208454324
|
A | G | 8 | a0001c0002t0002g0003a0001c0002t0002g0202a0001c0002t0002g0203others(5): Show | 10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.914+3515A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454324 | ||||||
chr2:208454461
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.914+3652G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454461 | ||||||
chr2:208454541
|
C | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.914+3732C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454541 | ||||||
chr2:208454708
|
T | C | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914+3899T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454708 | ||||||
chr2:208454967
|
A | G | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+4158A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208454967 | ||||||
chr2:208455268
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.914+4459G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455268 | ||||||
chr2:208455455
|
T | G | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.915-4440T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455455 | ||||||
chr2:208455475
|
C | T | 224 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(221): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.915-4420C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455475 | ||||||
chr2:208455551
|
C | G | 1 | a0006c0009t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.915-4344C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455551 | ||||||
chr2:208455573
|
G | T | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.915-4322G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455573 | ||||||
chr2:208455575
|
A | T | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.915-4320A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455575 | ||||||
chr2:208455783
|
ATTT | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019 | 4 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.915-4111_915-4109d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455783 | ||||||
chr2:208455883
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.915-4012A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455883 | ||||||
chr2:208455904
|
T | G | 1 | a0001c0001t0001g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.915-3991T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455904 | ||||||
chr2:208455931
|
T | C | 8 | a0001c0002t0002g0071a0001c0002t0002g0072a0001c0002t0002g0079others(5): Show | 8 | HG00438.hp1 HG00621.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.915-3964T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208455931 | ||||||
chr2:208456103
|
G | A | 2 | a0001c0002t0002g0084a0001c0003t0003g0030 | 2 | HG02145.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.915-3792G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456103 | ||||||
chr2:208456107
|
T | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0260a0001c0001t0001g0261others(14): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.915-3788T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456107 | ||||||
chr2:208456113
|
G | A | 1 | a0001c0002t0002g0080 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.915-3782G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456113 | ||||||
chr2:208456167
|
G | C | 3 | a0001c0001t0001g0141a0001c0001t0005g0140a0001c0001t0005g0142 | 3 | HG02486.hp2 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.915-3728G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456167 | ||||||
chr2:208456231
|
G | A | 28 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0003g0095others(25): Show | 28 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-3664G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456231 | ||||||
chr2:208456253
|
G | A | 28 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0003g0095others(25): Show | 28 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-3642G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456253 | ||||||
chr2:208456369
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.915-3526G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456369 | ||||||
chr2:208456421
|
A | G | 1 | a0001c0001t0001g0004 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915-3474A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456421 | ||||||
chr2:208456876
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.915-3019T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208456876 | ||||||
chr2:208457196
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.915-2699C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457196 | ||||||
chr2:208457271
|
G | T | 1 | a0001c0002t0002g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.915-2624G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457271 | ||||||
chr2:208457387
|
A | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.915-2508A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457387 | ||||||
chr2:208457461
|
G | T | 1 | a0001c0002t0002g0059 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.915-2434G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457461 | ||||||
chr2:208457482
|
T | C | 42 | a0001c0001t0001g0174a0001c0001t0001g0260a0001c0001t0001g0261others(39): Show | 43 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.915-2413T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457482 | ||||||
chr2:208457530
|
A | G | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-2365A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457530 | ||||||
chr2:208457587
|
G | A | 3 | a0001c0001t0003g0158a0001c0001t0003g0164a0007c0012t0003g0163 | 3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.915-2308G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457587 | ||||||
chr2:208457825
|
G | A | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.915-2070G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457825 | ||||||
chr2:208457991
|
T | A | 1 | a0001c0002t0002g0247 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.915-1904T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208457991 | ||||||
chr2:208458119
|
G | A | 1 | a0001c0002t0002g0084 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.915-1776G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458119 | ||||||
chr2:208458257
|
C | CA | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.915-1633dupA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208458257 | |||||
chr2:208458320
|
C | T | 3 | a0001c0001t0003g0158a0001c0001t0003g0164a0007c0012t0003g0163 | 3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.915-1575C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458320 | ||||||
chr2:208458326
|
A | G | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.915-1569A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458326 | ||||||
chr2:208458338
|
C | T | 1 | a0001c0002t0002g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.915-1557C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458338 | ||||||
chr2:208458478
|
A | C | 4 | a0001c0002t0002g0012a0001c0002t0002g0068a0001c0002t0002g0069others(1): Show | 5 | NA18945.hp2 NA18971.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.915-1417A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458478 | ||||||
chr2:208458495
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0005g0140a0001c0001t0005g0142others(1): Show | 4 | HG02486.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1400G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458495 | ||||||
chr2:208458599
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(119): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.915-1296T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458599 | ||||||
chr2:208458610
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.915-1285C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458610 | ||||||
chr2:208458693
|
C | T | 151 | a0001c0001t0001g0174a0001c0001t0001g0260a0001c0001t0001g0261others(148): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.915-1202C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458693 | ||||||
chr2:208458828
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.915-1067G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458828 | ||||||
chr2:208458848
|
C | T | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.915-1047C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458848 | ||||||
chr2:208458889
|
A | G | 2 | a0001c0003t0003g0010a0001c0003t0003g0145 | 3 | HG01069.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.915-1006A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458889 | ||||||
chr2:208458974
|
A | G | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.915-921A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208458974 | ||||||
chr2:208458998
|
GTTC | G | 77 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.915-891_915-889del others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 208458998 | |||||
chr2:208459074
|
G | A | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.915-821G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459074 | ||||||
chr2:208459078
|
A | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.915-817A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459078 | ||||||
chr2:208459175
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.915-720T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459175 | ||||||
chr2:208459216
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.915-679G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459216 | ||||||
chr2:208459530
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.915-365G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459530 | ||||||
chr2:208459685
|
T | A | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.915-210T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 8/12 | chr2 | 208459685 | ||||||
chr2:208459964
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.981+3A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208459964 | ||||||
chr2:208460036
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.981+75C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460036 | ||||||
chr2:208460140
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+179A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460140 | ||||||
chr2:208460905
|
G | C | 1 | a0001c0001t0003g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.981+944G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208460905 | ||||||
chr2:208461479
|
T | C | 1 | a0001c0002t0002g0112 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.981+1518T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461479 | ||||||
chr2:208461561
|
G | A | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+1600G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461561 | ||||||
chr2:208461627
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+1666T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461627 | ||||||
chr2:208461659
|
T | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+1698T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461659 | ||||||
chr2:208461738
|
G | A | 1 | a0001c0003t0003g0264 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.981+1777G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461738 | ||||||
chr2:208461792
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+1831C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461792 | ||||||
chr2:208461830
|
T | G | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.981+1869T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208461830 | ||||||
chr2:208462116
|
G | A | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.981+2155G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462116 | ||||||
chr2:208462125
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+2164A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462125 | ||||||
chr2:208462634
|
C | T | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.981+2673C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462634 | ||||||
chr2:208462880
|
G | A | 12 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(9): Show | 13 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.981+2919G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462880 | ||||||
chr2:208462979
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.981+3018G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462979 | ||||||
chr2:208462997
|
G | A | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+3036G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208462997 | ||||||
chr2:208463126
|
A | G | 1 | a0001c0001t0010g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+3165A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463126 | ||||||
chr2:208463353
|
C | T | 1 | a0006c0009t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.981+3392C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463353 | ||||||
chr2:208463470
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0190 | 2 | HG00423.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.981+3509G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463470 | ||||||
chr2:208463768
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.981+3807T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463768 | ||||||
chr2:208463817
|
T | A | 1 | a0005c0013t0001g0250 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981+3856T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463817 | ||||||
chr2:208463817
|
T | C | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+3856T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463817 | ||||||
chr2:208463858
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.981+3897G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463858 | ||||||
chr2:208463903
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+3942G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463903 | ||||||
chr2:208463968
|
A | T | 33 | a0001c0003t0003g0010a0001c0003t0003g0021a0001c0003t0003g0022others(30): Show | 34 | HG01069.hp2 HG01433.hp2 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.981+4007A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463968 | ||||||
chr2:208463988
|
A | T | 66 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0035others(63): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.981+4027A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463988 | ||||||
chr2:208463989
|
A | G | 1 | a0001c0003t0003g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.981+4028A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208463989 | ||||||
chr2:208464036
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.981+4075G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464036 | ||||||
chr2:208464144
|
G | T | 1 | a0001c0001t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.981+4183G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464144 | ||||||
chr2:208464231
|
A | G | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.981+4270A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464231 | ||||||
chr2:208464238
|
A | G | 18 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 19 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+4277A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464238 | ||||||
chr2:208464275
|
G | A | 1 | a0001c0003t0003g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.981+4314G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464275 | ||||||
chr2:208464329
|
A | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.981+4368A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464329 | ||||||
chr2:208464408
|
C | T | 2 | a0001c0003t0003g0034a0001c0003t0003g0149 | 2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.981+4447C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464408 | ||||||
chr2:208464453
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.981+4492A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464453 | ||||||
chr2:208464527
|
G | A | 4 | a0001c0002t0002g0122a0001c0002t0002g0123a0001c0002t0002g0124others(1): Show | 4 | NA18960.hp1 NA18990.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+4566G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464527 | ||||||
chr2:208464568
|
G | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+4607G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464568 | ||||||
chr2:208464599
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+4638C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464599 | ||||||
chr2:208464614
|
T | C | 6 | a0001c0003t0003g0015a0001c0003t0003g0264a0001c0003t0003g0266others(3): Show | 7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.981+4653T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464614 | ||||||
chr2:208464718
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.981+4757A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464718 | ||||||
chr2:208464736
|
G | A | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+4775G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464736 | ||||||
chr2:208464794
|
G | A | 1 | a0001c0002t0002g0194 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.981+4833G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464794 | ||||||
chr2:208464882
|
A | T | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+4921A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464882 | ||||||
chr2:208464938
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.981+4977T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464938 | ||||||
chr2:208464958
|
C | T | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.981+4997C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208464958 | ||||||
chr2:208465119
|
G | A | 1 | a0001c0002t0002g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.981+5158G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465119 | ||||||
chr2:208465272
|
A | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.981+5311A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465272 | ||||||
chr2:208465306
|
T | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(196): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.981+5345T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465306 | ||||||
chr2:208465332
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.981+5371C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465332 | ||||||
chr2:208465388
|
C | CT | 12 | a0001c0002t0002g0058a0001c0002t0002g0060a0001c0002t0002g0063others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.981+5459dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465388
|
C | CTT | 9 | a0001c0002t0002g0069a0001c0002t0002g0072a0001c0002t0002g0078others(6): Show | 9 | HG02027.hp2 HG02083.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+5458_981+5459d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465388
|
CT | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(54): Show | 61 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.981+5459delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465388
|
CTT | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.981+5458_981+5459d others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465388
|
CTTT | C | 18 | a0001c0001t0001g0091a0001c0003t0003g0020a0001c0003t0003g0023others(15): Show | 18 | HG01433.hp2 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.981+5457_981+5459d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465388
|
CTTTT | C | 10 | a0001c0001t0005g0140a0001c0003t0003g0021a0001c0003t0003g0022others(7): Show | 10 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+5456_981+5459d others(6): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465388 | |||||
chr2:208465663
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.981+5702A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465663 | ||||||
chr2:208465715
|
T | A | 9 | a0001c0001t0005g0142a0001c0002t0002g0068a0001c0002t0002g0069others(6): Show | 9 | HG02486.hp1 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+5754T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465715 | ||||||
chr2:208465893
|
TA | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0137 | 3 | HG01516.hp1 HG02895.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.981+5937delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208465893 | |||||
chr2:208465894
|
A | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.981+5933A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465894 | ||||||
chr2:208465895
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.981+5934A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208465895 | ||||||
chr2:208466090
|
T | G | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+6129T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466090 | ||||||
chr2:208466385
|
T | C | 1 | a0001c0001t0003g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.981+6424T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466385 | ||||||
chr2:208466391
|
T | C | 1 | a0001c0002t0002g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.981+6430T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466391 | ||||||
chr2:208466548
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.981+6587G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466548 | ||||||
chr2:208466763
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.981+6802C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466763 | ||||||
chr2:208466776
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.981+6815A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466776 | ||||||
chr2:208466862
|
T | C | 1 | a0001c0003t0003g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.981+6901T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466862 | ||||||
chr2:208466918
|
G | A | 3 | a0001c0001t0003g0158a0001c0001t0003g0164a0007c0012t0003g0163 | 3 | HG03490.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.981+6957G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208466918 | ||||||
chr2:208467202
|
T | A | 2 | a0001c0003t0003g0010a0001c0003t0003g0145 | 3 | HG01069.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.981+7241T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467202 | ||||||
chr2:208467408
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 5 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+7447A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467408 | ||||||
chr2:208467473
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0120others(15): Show | 22 | HG00597.hp1 HG02148.hp2 NA18940.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+7512A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467473 | ||||||
chr2:208467706
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.981+7745G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467706 | ||||||
chr2:208467730
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.981+7769T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467730 | ||||||
chr2:208467737
|
CA | C | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+7777delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467737 | ||||||
chr2:208467796
|
AAAG | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0229 | 3 | HG02083.hp2 NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981+7837_981+7839d others(5): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208467796 | |||||
chr2:208467801
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0229 | 3 | HG02083.hp2 NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981+7840C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467801 | ||||||
chr2:208467854
|
A | G | 1 | a0005c0013t0001g0250 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981+7893A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208467854 | ||||||
chr2:208468373
|
A | T | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+8412A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468373 | ||||||
chr2:208468454
|
G | A | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.981+8493G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468454 | ||||||
chr2:208468533
|
C | T | 2 | a0001c0002t0002g0007a0001c0002t0002g0119 | 3 | HG02109.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.981+8572C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468533 | ||||||
chr2:208468689
|
C | T | 25 | a0001c0001t0001g0174a0001c0001t0001g0206a0001c0001t0003g0095others(22): Show | 25 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.981+8728C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468689 | ||||||
chr2:208468770
|
T | C | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.981+8809T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468770 | ||||||
chr2:208468937
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.981+8976T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208468937 | ||||||
chr2:208469407
|
T | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.981+9446T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469407 | ||||||
chr2:208469704
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 5 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.981+9743A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469704 | ||||||
chr2:208469903
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.981+9942G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469903 | ||||||
chr2:208469943
|
A | G | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+9982A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208469943 | ||||||
chr2:208470046
|
T | C | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.981+10085T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470046 | ||||||
chr2:208470135
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.981+10174C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470135 | ||||||
chr2:208470205
|
C | T | 1 | a0001c0001t0001g0009 | 2 | NA18942.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.981+10244C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470205 | ||||||
chr2:208470206
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0257 | 2 | NA18970.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.981+10245G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470206 | ||||||
chr2:208470253
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.981+10292A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470253 | ||||||
chr2:208470361
|
A | G | 1 | a0001c0002t0002g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.981+10400A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470361 | ||||||
chr2:208470402
|
ATCTCATC others(255): Show |
A | 1 | a0001c0003t0003g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981+10444_982-1040 others(4): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208470402 | |||||
chr2:208470487
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(120): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.981+10526C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470487 | ||||||
chr2:208470565
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.982-10505C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470565 | ||||||
chr2:208470621
|
G | T | 2 | a0001c0006t0001g0040a0001c0006t0005g0144 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.982-10449G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470621 | ||||||
chr2:208470699
|
C | G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-10371C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470699 | ||||||
chr2:208470771
|
G | A | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-10299G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470771 | ||||||
chr2:208470964
|
G | A | 1 | a0001c0001t0003g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.982-10106G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208470964 | ||||||
chr2:208471044
|
A | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-10026A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208471044 | ||||||
chr2:208471458
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.982-9612T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208471458 | ||||||
chr2:208472036
|
A | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.982-9034A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472036 | ||||||
chr2:208472247
|
G | A | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-8823G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472247 | ||||||
chr2:208472688
|
T | A | 37 | a0001c0003t0003g0015a0001c0003t0003g0020a0001c0003t0003g0021others(34): Show | 38 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.982-8382T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472688 | ||||||
chr2:208472744
|
A | G | 1 | a0001c0001t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.982-8326A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208472744 | ||||||
chr2:208472895
|
TA | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.982-8173delA | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208472895 | |||||
chr2:208473012
|
T | G | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.982-8058T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473012 | ||||||
chr2:208473674
|
C | T | 2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.982-7396C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473674 | ||||||
chr2:208473888
|
G | A | 6 | a0001c0011t0004g0258a0002c0004t0004g0268a0002c0004t0004g0271others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-7182G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208473888 | ||||||
chr2:208474010
|
C | G | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-7060C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474010 | ||||||
chr2:208474033
|
A | G | 42 | a0001c0003t0003g0010a0001c0003t0003g0015a0001c0003t0003g0020others(39): Show | 44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.982-7037A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474033 | ||||||
chr2:208474166
|
T | C | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-6904T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474166 | ||||||
chr2:208474258
|
A | G | 12 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(9): Show | 12 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.982-6812A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474258 | ||||||
chr2:208474274
|
C | CA | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.982-6796_982-6795i others(3): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474274 | ||||||
chr2:208474477
|
A | T | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982-6593A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474477 | ||||||
chr2:208474488
|
C | G | 45 | a0001c0001t0005g0140a0001c0001t0005g0142a0001c0003t0003g0010others(42): Show | 47 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.982-6582C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474488 | ||||||
chr2:208474526
|
G | A | 8 | a0001c0001t0001g0191a0001c0001t0001g0208a0001c0001t0001g0210others(5): Show | 8 | HG01943.hp1 HG01993.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-6544G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474526 | ||||||
chr2:208474792
|
G | T | 3 | a0001c0001t0005g0140a0001c0001t0005g0142a0001c0006t0005g0144 | 3 | HG02258.hp1 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-6278G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474792 | ||||||
chr2:208474919
|
A | T | 1 | a0001c0001t0010g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-6151A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474919 | ||||||
chr2:208474978
|
C | T | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-6092C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208474978 | ||||||
chr2:208475092
|
A | G | 2 | a0001c0003t0003g0034a0001c0003t0003g0149 | 2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.982-5978A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475092 | ||||||
chr2:208475187
|
A | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.982-5883A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475187 | ||||||
chr2:208475188
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.982-5882A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475188 | ||||||
chr2:208475732
|
T | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-5338T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208475732 | ||||||
chr2:208476057
|
G | A | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-5013G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476057 | ||||||
chr2:208476130
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.982-4940A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476130 | ||||||
chr2:208476162
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.982-4908A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476162 | ||||||
chr2:208476199
|
G | C | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.982-4871G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476199 | ||||||
chr2:208476280
|
T | C | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-4790T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476280 | ||||||
chr2:208476423
|
A | G | 2 | a0001c0003t0003g0029a0001c0003t0003g0031 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.982-4647A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476423 | ||||||
chr2:208476501
|
G | T | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.982-4569G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476501 | ||||||
chr2:208476790
|
G | A | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.982-4280G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208476790 | ||||||
chr2:208477369
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.982-3701A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477369 | ||||||
chr2:208477392
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.982-3678C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477392 | ||||||
chr2:208477458
|
T | G | 1 | a0006c0009t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.982-3612T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477458 | ||||||
chr2:208477581
|
C | A | 15 | a0001c0003t0003g0021a0001c0003t0003g0022a0001c0003t0003g0023others(12): Show | 15 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.982-3489C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477581 | ||||||
chr2:208477690
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.982-3380T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477690 | ||||||
chr2:208477764
|
CTTTGT | C | 8 | a0001c0003t0003g0015a0001c0003t0003g0259a0001c0003t0003g0263others(5): Show | 9 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-3300_982-3296d others(7): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477764 | |||||
chr2:208477880
|
T | TTACTACT others(11): Show |
10 | a0001c0002t0002g0003a0001c0002t0002g0202a0001c0002t0002g0203others(7): Show | 12 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-3142_982-3125d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477880 | |||||
chr2:208477880
|
TTACTACT others(11): Show |
T | 2 | a0001c0001t0005g0142a0001c0002t0002g0094 | 2 | NA18950.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.982-3142_982-3125d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477880 | |||||
chr2:208477882
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.982-3188A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477882 | ||||||
chr2:208477896
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.982-3174C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477896 | ||||||
chr2:208477916
|
C | CTACTACT others(20): Show |
1 | a0001c0003t0003g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.982-3151_982-3125d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477916 | |||||
chr2:208477937
|
CTACTAGT others(20): Show |
C | 2 | a0001c0003t0003g0148a0001c0003t0003g0152 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.982-3124_982-3098d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477937 | |||||
chr2:208477946
|
G | C | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-3124G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477946 | ||||||
chr2:208477946
|
G | GTACTAGC others(20): Show |
8 | a0001c0002t0002g0071a0001c0002t0002g0072a0001c0002t0002g0079others(5): Show | 8 | HG00438.hp1 HG00621.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-3091_982-3065d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477946 | |||||
chr2:208477946
|
GTACTAGC others(20): Show |
G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(120): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.982-3091_982-3065d others(29): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477946 | |||||
chr2:208477953
|
C | T | 6 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-3117C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477953 | ||||||
chr2:208477964
|
G | GTACTAGC others(5): Show |
1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.982-3100_982-3099i others(14): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477964 | |||||
chr2:208477970
|
GTACTACT others(8): Show |
G | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.982-3094_982-3080d others(17): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477970 | |||||
chr2:208477973
|
C | CTACTAGT others(11): Show |
2 | a0001c0003t0003g0038a0001c0003t0003g0039 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.982-3091_982-3090i others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477973 | |||||
chr2:208477973
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.982-3097C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477973 | ||||||
chr2:208477973
|
CTACTAGC others(11): Show |
C | 1 | a0001c0003t0003g0028 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.982-3090_982-3073d others(20): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 208477973 | |||||
chr2:208477980
|
C | T | 67 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(64): Show | 69 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.982-3090C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208477980 | ||||||
chr2:208478284
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-2786C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478284 | ||||||
chr2:208478493
|
G | A | 6 | a0001c0011t0004g0258a0002c0004t0004g0268a0002c0004t0004g0271others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-2577G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478493 | ||||||
chr2:208478534
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0244 | 2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.982-2536C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478534 | ||||||
chr2:208478739
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.982-2331C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478739 | ||||||
chr2:208478804
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.982-2266C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208478804 | ||||||
chr2:208479141
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.982-1929G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479141 | ||||||
chr2:208479184
|
G | T | 6 | a0001c0001t0003g0157a0001c0001t0003g0165a0001c0001t0003g0170others(3): Show | 6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-1886G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479184 | ||||||
chr2:208479196
|
C | T | 1 | a0001c0002t0002g0052 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.982-1874C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479196 | ||||||
chr2:208479242
|
G | T | 2 | a0001c0002t0002g0052a0001c0002t0002g0080 | 2 | NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.982-1828G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479242 | ||||||
chr2:208479288
|
G | A | 6 | a0001c0003t0003g0015a0001c0003t0003g0264a0001c0003t0003g0266others(3): Show | 7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-1782G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479288 | ||||||
chr2:208479490
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.982-1580C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479490 | ||||||
chr2:208479645
|
C | T | 1 | a0001c0002t0002g0082 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.982-1425C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208479645 | ||||||
chr2:208480069
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.982-1001C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480069 | ||||||
chr2:208480259
|
G | A | 7 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149others(4): Show | 7 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.982-811G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480259 | ||||||
chr2:208480271
|
A | G | 8 | a0001c0002t0002g0003a0001c0002t0002g0202a0001c0002t0002g0203others(5): Show | 10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.982-799A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480271 | ||||||
chr2:208480583
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(200): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.982-487G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480583 | ||||||
chr2:208480632
|
C | T | 1 | a0001c0001t0010g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-438C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480632 | ||||||
chr2:208480789
|
A | G | 1 | a0001c0003t0003g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.982-281A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480789 | ||||||
chr2:208480941
|
T | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.982-129T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 9/12 | chr2 | 208480941 | ||||||
chr2:208481219
|
CT | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1076+72delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208481219 | |||||
chr2:208481219
|
CTT | C | 27 | a0001c0001t0001g0120a0001c0001t0001g0174a0001c0001t0001g0193others(24): Show | 27 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.1076+71_1076+72del others(2): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208481219 | |||||
chr2:208481295
|
T | TGCAACCT others(1): Show |
192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1076+131_1076+132i others(10): Show |
PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481295 | ||||||
chr2:208481304
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG00323.hp1 HG01106.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1076+140G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481304 | ||||||
chr2:208481360
|
G | A | 1 | a0001c0003t0003g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1076+196G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481360 | ||||||
chr2:208481622
|
A | G | 42 | a0001c0003t0003g0010a0001c0003t0003g0015a0001c0003t0003g0020others(39): Show | 44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1076+458A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481622 | ||||||
chr2:208481864
|
G | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1076+700G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481864 | ||||||
chr2:208481939
|
T | C | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1076+775T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208481939 | ||||||
chr2:208482083
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076+919T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482083 | ||||||
chr2:208482267
|
T | C | 1 | a0001c0003t0003g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+1103T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482267 | ||||||
chr2:208482282
|
C | T | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+1118C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482282 | ||||||
chr2:208482379
|
A | G | 4 | a0001c0002t0002g0042a0001c0002t0002g0044a0001c0002t0002g0066others(1): Show | 4 | HG00609.hp2 NA18983.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1215A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482379 | ||||||
chr2:208482522
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1076+1358A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482522 | ||||||
chr2:208482745
|
T | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1076+1581T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482745 | ||||||
chr2:208482918
|
C | T | 1 | a0001c0002t0002g0189 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1076+1754C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208482918 | ||||||
chr2:208483079
|
G | T | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1076+1915G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483079 | ||||||
chr2:208483081
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1076+1917G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483081 | ||||||
chr2:208483380
|
G | T | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1076+2216G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483380 | ||||||
chr2:208483417
|
T | A | 33 | a0001c0003t0003g0010a0001c0003t0003g0021a0001c0003t0003g0022others(30): Show | 34 | HG01069.hp2 HG01433.hp2 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1076+2253T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483417 | ||||||
chr2:208483456
|
G | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1076+2292G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483456 | ||||||
chr2:208483575
|
G | A | 24 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(21): Show | 24 | HG01496.hp2 HG01884.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.1076+2411G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483575 | ||||||
chr2:208483586
|
A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1076+2422A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483586 | ||||||
chr2:208483672
|
C | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1076+2508C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483672 | ||||||
chr2:208483673
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1076+2509A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483673 | ||||||
chr2:208483687
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1076+2523T>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483687 | ||||||
chr2:208483899
|
G | A | 1 | a0001c0003t0003g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1076+2735G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208483899 | ||||||
chr2:208484170
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1076+3006T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484170 | ||||||
chr2:208484178
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+3014A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484178 | ||||||
chr2:208484203
|
C | T | 1 | a0001c0002t0002g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1076+3039C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484203 | ||||||
chr2:208484314
|
G | A | 1 | a0001c0006t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1076+3150G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484314 | ||||||
chr2:208484498
|
T | C | 14 | a0001c0003t0003g0015a0001c0003t0003g0020a0001c0003t0003g0259others(11): Show | 15 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1076+3334T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208484498 | ||||||
chr2:208485252
|
G | C | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-3760G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485252 | ||||||
chr2:208485339
|
C | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG02055.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1077-3673C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485339 | ||||||
chr2:208485403
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1077-3609G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485403 | ||||||
chr2:208485575
|
G | T | 1 | a0001c0003t0003g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1077-3437G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485575 | ||||||
chr2:208485582
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0120others(15): Show | 22 | HG00597.hp1 HG02148.hp2 NA18940.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077-3430C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485582 | ||||||
chr2:208485583
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1077-3429A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485583 | ||||||
chr2:208485658
|
G | T | 5 | a0001c0003t0003g0154a0001c0003t0003g0155a0001c0003t0003g0156others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077-3354G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485658 | ||||||
chr2:208485707
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1077-3305C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485707 | ||||||
chr2:208485901
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1077-3111C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208485901 | ||||||
chr2:208486021
|
G | A | 1 | a0001c0011t0004g0258 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1077-2991G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486021 | ||||||
chr2:208486600
|
A | T | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1077-2412A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486600 | ||||||
chr2:208486611
|
A | T | 1 | a0001c0002t0002g0007 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-2401A>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486611 | ||||||
chr2:208486732
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1077-2280A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208486732 | ||||||
chr2:208487211
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077-1801A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487211 | ||||||
chr2:208487433
|
C | T | 1 | a0001c0003t0003g0034 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1077-1579C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487433 | ||||||
chr2:208487600
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1412C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487600 | ||||||
chr2:208487687
|
G | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1325G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487687 | ||||||
chr2:208487725
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1077-1287C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487725 | ||||||
chr2:208487776
|
A | G | 25 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(22): Show | 25 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077-1236A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487776 | ||||||
chr2:208487813
|
C | T | 25 | a0001c0001t0001g0174a0001c0001t0003g0095a0001c0001t0003g0157others(22): Show | 25 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077-1199C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487813 | ||||||
chr2:208487874
|
G | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-1138G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208487874 | ||||||
chr2:208488141
|
G | A | 1 | a0001c0003t0003g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1077-871G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488141 | ||||||
chr2:208488210
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-802C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488210 | ||||||
chr2:208488447
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077-565A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488447 | ||||||
chr2:208488487
|
A | AT | 2 | a0001c0001t0001g0005a0001c0001t0001g0019 | 3 | HG02257.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1077-521dupT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208488487 | |||||
chr2:208488526
|
G | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-486G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488526 | ||||||
chr2:208488702
|
C | T | 3 | a0001c0003t0003g0034a0001c0003t0003g0143a0001c0003t0003g0149 | 3 | HG01433.hp2 HG02258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1077-310C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488702 | ||||||
chr2:208488826
|
G | C | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077-186G>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488826 | ||||||
chr2:208488833
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1077-179C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488833 | ||||||
chr2:208488882
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1077-130A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488882 | ||||||
chr2:208488931
|
GT | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1077-71delT | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 208488931 | |||||
chr2:208488951
|
C | A | 6 | a0001c0002t0002g0003a0001c0002t0002g0203a0001c0002t0002g0204others(3): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077-61C>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488951 | ||||||
chr2:208488969
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077-43G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 10/12 | chr2 | 208488969 | ||||||
chr2:208489719
|
T | G | 1 | a0001c0001t0006g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1215+569T>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208489719 | ||||||
chr2:208490132
|
C | T | 1 | a0001c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1216-507C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208490132 | ||||||
chr2:208490580
|
T | C | 4 | a0001c0003t0003g0150a0001c0003t0003g0153a0001c0008t0003g0146others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-59T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 11/12 | chr2 | 208490580 | ||||||
chr2:208490853
|
A | G | 8 | a0001c0002t0002g0003a0001c0002t0002g0202a0001c0002t0002g0203others(5): Show | 10 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+173A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208490853 | ||||||
chr2:208490939
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1257+259A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208490939 | ||||||
chr2:208491203
|
A | G | 1 | a0001c0002t0002g0205 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1257+523A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491203 | ||||||
chr2:208491215
|
G | T | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1257+535G>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491215 | ||||||
chr2:208491222
|
G | A | 9 | a0001c0003t0003g0015a0001c0003t0003g0020a0001c0003t0003g0259others(6): Show | 10 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+542G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491222 | ||||||
chr2:208491252
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1257+572G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491252 | ||||||
chr2:208491529
|
A | G | 2 | a0001c0002t0002g0067a0001c0002t0002g0098 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1257+849A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491529 | ||||||
chr2:208491675
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1257+995C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491675 | ||||||
chr2:208491676
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1257+996C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491676 | ||||||
chr2:208491683
|
C | G | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1257+1003C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491683 | ||||||
chr2:208491691
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1257+1011C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491691 | ||||||
chr2:208491847
|
A | C | 2 | a0001c0003t0003g0015a0001c0003t0003g0267 | 3 | HG00735.hp1 HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1257+1167A>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208491847 | ||||||
chr2:208492195
|
C | T | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1258-1069C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492195 | ||||||
chr2:208492198
|
G | A | 1 | a0001c0006t0005g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1258-1066G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492198 | ||||||
chr2:208492268
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0007g0187 | 2 | NA18978.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1258-996T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492268 | ||||||
chr2:208492554
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1258-710C>T | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492554 | ||||||
chr2:208492729
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1258-535T>C | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492729 | ||||||
chr2:208492746
|
A | G | 5 | a0002c0004t0004g0268a0002c0004t0004g0271a0002c0004t0004g0272others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-518A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492746 | ||||||
chr2:208492898
|
G | A | 1 | a0004c0007t0001g0008 | 2 | NA18952.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1258-366G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492898 | ||||||
chr2:208492918
|
A | G | 1 | a0001c0003t0003g0259 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1258-346A>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492918 | ||||||
chr2:208492947
|
C | G | 42 | a0001c0003t0003g0010a0001c0003t0003g0015a0001c0003t0003g0020others(39): Show | 44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-317C>G | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208492947 | ||||||
chr2:208493145
|
G | A | 42 | a0001c0003t0003g0010a0001c0003t0003g0015a0001c0003t0003g0020others(39): Show | 44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-119G>A | PTH2R | ENSG00000144407.10 | transcript | ENST00000272847.7 | protein_coding | 12/12 | chr2 | 208493145 |