geneid | 283554 |
---|---|
ensemblid | ENSG00000180998.12 |
hgncid | 25445 |
symbol | GPR137C |
name | G protein-coupled receptor 137C |
refseq_nuc | NM_001099652.2 |
refseq_prot | NP_001093122.1 |
ensembl_nuc | ENST00000321662.11 |
ensembl_prot | ENSP00000315106.6 |
mane_status | MANE Select |
chr | chr14 |
start | 52552836 |
end | 52637713 |
strand | + |
ver | v1.2 |
region | chr14:52552836-52637713 |
region5000 | chr14:52547836-52642713 |
regionname0 | GPR137C_chr14_52552836_52637713 |
regionname5000 | GPR137C_chr14_52547836_52642713 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 429 | 204 | 52 | 22 | 100 | 5 | 24 | 77 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002 | 0/0 | 429 | 88 | 13 | 20 | 38 | 7 | 10 | 28 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003 | 1/0 | 429 | 26 | 16 | 2 | 6 | 0 | 1 | 4 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0004 | 0/0 | 429 | 24 | 0 | 3 | 18 | 0 | 3 | 14 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0005 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0006 | 0/0 | 429 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0007 | 0/0 | 166 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0008 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1290 | 181 | 45 | 14 | 95 | 4 | 22 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0002 | 0/0 | 1290 | 88 | 13 | 20 | 38 | 7 | 10 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0003 | 1/0 | 1290 | 26 | 16 | 2 | 6 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0004 | 0/0 | 1290 | 24 | 0 | 3 | 18 | 0 | 3 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0005 | 0/0 | 1290 | 15 | 6 | 4 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0006 | 0/0 | 1290 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0007 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0008 | 0/0 | 1290 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0009 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0010 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
c0011 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2911 | 222 | 41 | 26 | 115 | 9 | 30 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0002 | 0/1 | 2911 | 32 | 7 | 8 | 10 | 2 | 4 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0003 | 0/0 | 2911 | 29 | 0 | 1 | 28 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0004 | 0/0 | 2911 | 11 | 11 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0005 | 0/0 | 2911 | 8 | 0 | 3 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0006 | 0/0 | 2911 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0007 | 0/0 | 2911 | 6 | 6 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0008 | 0/0 | 2911 | 4 | 1 | 0 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0009 | 0/0 | 2911 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0010 | 0/0 | 2911 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0011 | 0/0 | 2911 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0012 | 0/0 | 2911 | 3 | 0 | 2 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0013 | 0/0 | 2911 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0014 | 0/0 | 2911 | 2 | 0 | 1 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0015 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0016 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0017 | 0/0 | 2911 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0018 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0019 | 0/0 | 2911 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0020 | 0/0 | 2911 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0021 | 0/0 | 2911 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0022 | 0/0 | 2911 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0023 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0024 | 0/0 | 2929 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
t0025 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1290 | 181 | 45 | 14 | 95 | 4 | 22 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0005 | 0/0 | 1290 | 15 | 6 | 4 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0006 | 0/0 | 1290 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0007 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002 | 0/0 | 1290 | 88 | 13 | 20 | 38 | 7 | 10 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003 | 1/0 | 1290 | 26 | 16 | 2 | 6 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0004c0004 | 0/0 | 1290 | 24 | 0 | 3 | 18 | 0 | 3 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0005c0009 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0006c0008 | 0/0 | 1290 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0007c0010 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0008c0011 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4200 | 101 | 22 | 4 | 56 | 2 | 17 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0002 | 0/1 | 4200 | 26 | 5 | 7 | 7 | 2 | 4 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0003 | 0/0 | 4200 | 29 | 0 | 1 | 28 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0004 | 0/0 | 4200 | 11 | 11 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0008 | 0/0 | 4200 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0009 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0010 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0013 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0014 | 0/0 | 4200 | 2 | 0 | 1 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0015 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0016 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0019 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0021 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0022 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0001t0025 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0005t0005 | 0/0 | 4200 | 8 | 0 | 3 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0005t0007 | 0/0 | 4200 | 6 | 6 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0005t0017 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0006t0006 | 0/0 | 4200 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0001c0007t0008 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002t0001 | 0/0 | 4200 | 82 | 12 | 17 | 37 | 7 | 9 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002t0012 | 0/0 | 4200 | 3 | 0 | 2 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002t0018 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002t0020 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0002c0002t0024 | 0/0 | 4218 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0001 | 1/0 | 4200 | 13 | 7 | 1 | 3 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0002 | 0/0 | 4200 | 5 | 1 | 1 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0009 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0010 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0011 | 0/0 | 4200 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0003c0003t0023 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0004c0004t0001 | 0/0 | 4200 | 23 | 0 | 3 | 17 | 0 | 3 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0004c0004t0008 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0005c0009t0001 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0006c0008t0001 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0007c0010t0001 | 0/0 | 4246 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
a0008c0011t0002 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | copy fasta | chr14 | 52547836 | 52642713 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0008g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0014g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0014g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0016g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0019g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0021g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0022g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0001t0025g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0007g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0005t0017g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0006t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0001c0007t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0012g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0012g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0018g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0020g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0002c0002t0024g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0010g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0003c0003t0023g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0004c0004t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0005c0009t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0006c0008t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0007c0010t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
a0008c0011t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0118 | EUR | GBR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0052 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0066 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0116 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00408 | hp2 | a0004 | c0004 | t0001 | g0271 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00621 | hp1 | a0001 | c0001 | t0008 | g0304 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00621 | hp2 | a0003 | c0003 | t0002 | g0130 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00639 | hp2 | a0001 | c0001 | t0014 | g0235 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00642 | hp1 | a0001 | c0006 | t0006 | g0163 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00735 | hp1 | a0004 | c0004 | t0001 | g0042 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00735 | hp2 | a0001 | c0006 | t0006 | g0157 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00738 | hp1 | a0002 | c0002 | t0020 | g0144 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG00738 | hp2 | a0001 | c0005 | t0005 | g0200 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01074 | hp2 | a0006 | c0008 | t0001 | g0173 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01099 | hp2 | a0002 | c0002 | t0012 | g0051 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01168 | hp1 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01169 | hp1 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01243 | hp2 | a0001 | c0005 | t0017 | g0293 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01257 | hp1 | a0001 | c0006 | t0006 | g0159 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01258 | hp1 | a0002 | c0002 | t0012 | g0109 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0134 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01496 | hp1 | a0004 | c0004 | t0001 | g0025 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0086 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01515 | hp2 | a0001 | c0006 | t0006 | g0162 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0087 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01943 | hp2 | a0001 | c0006 | t0006 | g0158 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01978 | hp2 | a0001 | c0001 | t0021 | g0179 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01993 | hp1 | a0004 | c0004 | t0001 | g0020 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG01993 | hp2 | a0003 | c0003 | t0002 | g0071 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02015 | hp1 | a0004 | c0004 | t0001 | g0273 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02040 | hp2 | a0007 | c0010 | t0001 | g0248 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0192 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02132 | hp2 | a0004 | c0004 | t0001 | g0023 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02257 | hp1 | a0008 | c0011 | t0002 | g0174 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02258 | hp2 | a0001 | c0007 | t0008 | g0156 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0143 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02615 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02622 | hp1 | a0003 | c0003 | t0023 | g0281 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02717 | hp1 | a0003 | c0003 | t0011 | g0284 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02717 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02723 | hp1 | a0003 | c0003 | t0009 | g0047 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02818 | hp1 | a0001 | c0005 | t0007 | g0297 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02818 | hp2 | a0002 | c0002 | t0018 | g0081 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0167 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02895 | hp2 | a0003 | c0003 | t0009 | g0048 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0170 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02965 | hp1 | a0003 | c0003 | t0011 | g0283 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03041 | hp1 | a0001 | c0005 | t0007 | g0296 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03130 | hp1 | a0003 | c0003 | t0011 | g0282 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03130 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03195 | hp2 | a0001 | c0001 | t0025 | g0193 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03239 | hp2 | a0004 | c0004 | t0001 | g0041 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03453 | hp2 | a0003 | c0003 | t0010 | g0285 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03490 | hp1 | a0001 | c0001 | t0014 | g0236 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03491 | hp1 | a0001 | c0006 | t0006 | g0161 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03579 | hp1 | a0003 | c0003 | t0010 | g0286 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0230 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0061 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04199 | hp1 | a0004 | c0004 | t0001 | g0267 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04204 | hp1 | a0002 | c0002 | t0012 | g0050 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18747 | hp1 | a0004 | c0004 | t0001 | g0263 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18947 | hp2 | a0004 | c0004 | t0001 | g0268 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18953 | hp2 | a0004 | c0004 | t0001 | g0274 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18957 | hp2 | a0001 | c0005 | t0005 | g0204 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18965 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18966 | hp2 | a0001 | c0005 | t0005 | g0203 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18975 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18977 | hp2 | a0004 | c0004 | t0001 | g0258 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18980 | hp2 | a0001 | c0001 | t0019 | g0038 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18985 | hp1 | a0001 | c0005 | t0005 | g0202 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18985 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18991 | hp1 | a0002 | c0002 | t0024 | g0135 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18992 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA18999 | hp2 | a0004 | c0004 | t0008 | g0315 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19003 | hp1 | a0004 | c0004 | t0001 | g0039 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19003 | hp2 | a0005 | c0009 | t0001 | g0269 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19007 | hp1 | a0001 | c0005 | t0005 | g0007 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0310 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19012 | hp1 | a0004 | c0004 | t0001 | g0033 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19058 | hp1 | a0004 | c0004 | t0001 | g0201 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19063 | hp2 | a0001 | c0005 | t0005 | g0007 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19083 | hp1 | a0004 | c0004 | t0001 | g0018 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19086 | hp1 | a0001 | c0001 | t0022 | g0291 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19087 | hp1 | a0004 | c0004 | t0001 | g0246 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19087 | hp2 | a0004 | c0004 | t0001 | g0044 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ASW | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20129 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ASW | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0331 | EUR | TSI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20905 | hp1 | a0001 | c0006 | t0006 | g0160 | SAS | GIH | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | GIH | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0217 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0168 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20300 | hp1 | a0001 | c0005 | t0007 | g0295 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0072 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0172 | AFR | LWK | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0195 | REF | REF | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0110 | REF | REF | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52553226
|
A | G | 6 | a0001a0004a0005others(3): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
missense_variant | MODERATE | c.79A>G | p.Ser27Gly | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 391/4200 | 79/1290 | 27/429 | chr14 | 52553226 | ||
chr14:52553246
|
CGCTGCAG others(14): Show |
C | 1 | a0008 | 1 | HG02257.hp1 | disruptive_inframe_deletion | MODERATE | c.101_121delCTGCAGCC others(13): Show |
p.Ala34_Ala40del | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 413/4200 | 101/1290 | 34/429 | INFO_REALIGN_3_PRIME | chr14 | 52553246 | |
chr14:52553256
|
T | TCCCCCCC others(39): Show |
1 | a0007 | 1 | HG02040.hp2 | frameshift_variant | HIGH | c.110_111insCCCCCCCT others(38): Show |
p.Gly38fs | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 423/4200 | 111/1290 | 37/429 | INFO_REALIGN_3_PRIME | chr14 | 52553256 | |
chr14:52553259
|
G | C | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.112G>C | p.Gly38Arg | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 424/4200 | 112/1290 | 38/429 | chr14 | 52553259 | ||
chr14:52553260
|
G | C | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.113G>C | p.Gly38Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 425/4200 | 113/1290 | 38/429 | chr14 | 52553260 | ||
chr14:52553262
|
G | C | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.115G>C | p.Ala39Pro | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 427/4200 | 115/1290 | 39/429 | chr14 | 52553262 | ||
chr14:52553271
|
C | G | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.124C>G | p.Pro42Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 436/4200 | 124/1290 | 42/429 | chr14 | 52553271 | ||
chr14:52553559
|
A | G | 1 | a0005 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.412A>G | p.Thr138Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 724/4200 | 412/1290 | 138/429 | chr14 | 52553559 | ||
chr14:52553560
|
C | T | 1 | a0006 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.413C>T | p.Thr138Met | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 725/4200 | 413/1290 | 138/429 | chr14 | 52553560 | ||
chr14:52632184
|
G | A | 2 | a0002a0004 | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
missense_variant | MODERATE | c.742G>A | p.Val248Ile | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/7 | 1054/4200 | 742/1290 | 248/429 | chr14 | 52632184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52553228
|
C | T | 1 | a0001c0006 | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
synonymous_variant | LOW | c.81C>T | p.Ser27Ser | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 393/4200 | 81/1290 | 27/429 | chr14 | 52553228 | ||
chr14:52553258
|
A | C | 1 | a0007c0010 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.111A>C | p.Ser37Ser | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 423/4200 | 111/1290 | 37/429 | chr14 | 52553258 | ||
chr14:52553273
|
G | C | 1 | a0007c0010 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.126G>C | p.Pro42Pro | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 438/4200 | 126/1290 | 42/429 | chr14 | 52553273 | ||
chr14:52553561
|
G | C | 1 | a0006c0008 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.414G>C | p.Thr138Thr | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 726/4200 | 414/1290 | 138/429 | chr14 | 52553561 | ||
chr14:52632210
|
G | C | 1 | a0001c0005 | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.768G>C | p.Leu256Leu | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/7 | 1080/4200 | 768/1290 | 256/429 | chr14 | 52632210 | ||
chr14:52633881
|
C | T | 1 | a0001c0007 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1047C>T | p.Phe349Phe | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/7 | 1359/4200 | 1047/1290 | 349/429 | chr14 | 52633881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52552902
|
T | C | 1 | a0001c0006t0006 | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-246T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | chr14 | 52552902 | ||||||
chr14:52552922
|
C | G | 1 | a0002c0002t0012 | 3 | HG01099.hp2 HG01258.hp1 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-226C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 226 | chr14 | 52552922 | |||||
chr14:52552989
|
G | A | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(2): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-159G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 159 | chr14 | 52552989 | |||||
chr14:52635133
|
G | A | 1 | a0001c0001t0015 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 18 | chr14 | 52635133 | |||||
chr14:52635282
|
A | G | 1 | a0001c0001t0025 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 167 | chr14 | 52635282 | |||||
chr14:52635359
|
A | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 244 | chr14 | 52635359 | |||||
chr14:52635363
|
A | AACCCCCC others(61): Show |
1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248_*249insACCCCC others(62): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 249 | chr14 | 52635363 | |||||
chr14:52635364
|
T | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*249T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 249 | chr14 | 52635364 | |||||
chr14:52635366
|
CTGACTTT others(43): Show |
C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252_*301delTGACTT others(44): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 252 | chr14 | 52635366 | |||||
chr14:52635418
|
A | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 303 | chr14 | 52635418 | |||||
chr14:52635419
|
C | T | 4 | a0001c0001t0010a0003c0003t0010a0003c0003t0011others(1): Show | 7 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 304 | chr14 | 52635419 | |||||
chr14:52635684
|
A | G | 1 | a0001c0001t0022 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 569 | chr14 | 52635684 | |||||
chr14:52635704
|
G | A | 1 | a0001c0001t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 589 | chr14 | 52635704 | |||||
chr14:52635733
|
G | A | 1 | a0001c0001t0013 | 2 | HG02886.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*618G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 618 | chr14 | 52635733 | |||||
chr14:52635743
|
G | A | 1 | a0001c0005t0017 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 628 | chr14 | 52635743 | |||||
chr14:52635941
|
T | C | 1 | a0002c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 826 | chr14 | 52635941 | |||||
chr14:52635966
|
A | C | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 76 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*851A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 851 | chr14 | 52635966 | |||||
chr14:52636081
|
C | T | 1 | a0002c0002t0020 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 966 | chr14 | 52636081 | |||||
chr14:52636268
|
T | C | 2 | a0001c0001t0010a0003c0003t0010 | 3 | HG03453.hp2 HG03579.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1153 | chr14 | 52636268 | |||||
chr14:52636425
|
G | A | 1 | a0001c0001t0014 | 2 | HG00639.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1310G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1310 | chr14 | 52636425 | |||||
chr14:52636754
|
A | C | 1 | a0003c0003t0023 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1639 | chr14 | 52636754 | |||||
chr14:52636838
|
G | A | 5 | a0001c0001t0002a0001c0001t0003a0001c0001t0021others(2): Show | 62 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1723G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1723 | chr14 | 52636838 | |||||
chr14:52636956
|
A | G | 3 | a0001c0005t0005a0001c0005t0007a0001c0005t0017 | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1841A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1841 | chr14 | 52636956 | |||||
chr14:52636995
|
G | T | 1 | a0001c0001t0019 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1880G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1880 | chr14 | 52636995 | |||||
chr14:52637035
|
C | T | 1 | a0001c0001t0021 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1920 | chr14 | 52637035 | |||||
chr14:52637671
|
T | C | 1 | a0001c0005t0005 | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2556T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 2556 | chr14 | 52637671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:52553905
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.444+314C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52553905 | ||||||
chr14:52553974
|
G | A | 1 | a0002c0002t0001g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.444+383G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52553974 | ||||||
chr14:52554002
|
C | T | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+411C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554002 | ||||||
chr14:52554154
|
C | G | 32 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(29): Show | 32 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.444+563C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554154 | ||||||
chr14:52554164
|
T | C | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.444+573T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554164 | ||||||
chr14:52554373
|
A | G | 1 | a0001c0001t0003g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.444+782A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554373 | ||||||
chr14:52554389
|
C | T | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.444+798C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554389 | ||||||
chr14:52554457
|
G | C | 1 | a0002c0002t0001g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.444+866G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554457 | ||||||
chr14:52554550
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444+959A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554550 | ||||||
chr14:52554671
|
C | T | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+1080C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554671 | ||||||
chr14:52554713
|
TA | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 240 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.444+1136delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52554713 | |||||
chr14:52554715
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+1124A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554715 | ||||||
chr14:52554790
|
T | A | 2 | a0003c0003t0009g0047a0003c0003t0009g0048 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.444+1199T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554790 | ||||||
chr14:52554825
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+1234G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554825 | ||||||
chr14:52555229
|
C | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+1638C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555229 | ||||||
chr14:52555465
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+1874C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555465 | ||||||
chr14:52555841
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+2250C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555841 | ||||||
chr14:52555956
|
A | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 4 | NA18959.hp2 NA18993.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+2365A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555956 | ||||||
chr14:52555992
|
T | G | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+2401T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555992 | ||||||
chr14:52556001
|
T | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+2410T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556001 | ||||||
chr14:52556030
|
C | T | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.444+2439C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556030 | ||||||
chr14:52556117
|
C | T | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+2526C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556117 | ||||||
chr14:52556119
|
T | G | 16 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(13): Show | 16 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+2528T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556119 | ||||||
chr14:52556148
|
G | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(79): Show | 85 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.444+2557G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556148 | ||||||
chr14:52556171
|
G | A | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+2580G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556171 | ||||||
chr14:52556376
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.444+2785C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556376 | ||||||
chr14:52556391
|
C | CT | 229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.444+2813dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52556391 | |||||
chr14:52556416
|
C | T | 26 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0002g0005others(23): Show | 28 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+2825C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556416 | ||||||
chr14:52556509
|
TGA | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+2926_444+2927d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52556509 | |||||
chr14:52556565
|
C | G | 8 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0138others(5): Show | 8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+2974C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556565 | ||||||
chr14:52556796
|
T | G | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+3205T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556796 | ||||||
chr14:52556847
|
A | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+3256A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556847 | ||||||
chr14:52556865
|
A | G | 2 | a0003c0003t0001g0133a0003c0003t0001g0134 | 2 | HG01433.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+3274A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556865 | ||||||
chr14:52556889
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(174): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.444+3298G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556889 | ||||||
chr14:52557039
|
T | C | 2 | a0002c0002t0012g0050a0002c0002t0012g0051 | 2 | HG01099.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.444+3448T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557039 | ||||||
chr14:52557129
|
T | C | 177 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 184 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.444+3538T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557129 | ||||||
chr14:52557196
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+3605C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557196 | ||||||
chr14:52557197
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+3606A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557197 | ||||||
chr14:52557400
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+3809A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557400 | ||||||
chr14:52557628
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.444+4037C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557628 | ||||||
chr14:52557658
|
G | A | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+4067G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557658 | ||||||
chr14:52557739
|
A | G | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+4148A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557739 | ||||||
chr14:52557888
|
T | G | 1 | a0001c0006t0006g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.444+4297T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557888 | ||||||
chr14:52558103
|
C | A | 1 | a0004c0004t0001g0013 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.444+4512C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558103 | ||||||
chr14:52558103
|
C | CA | 106 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(103): Show | 109 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.444+4527dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52558103 | |||||
chr14:52558103
|
C | CAAA | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+4525_444+4527d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52558103 | |||||
chr14:52558148
|
GT | G | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+4558delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558148 | ||||||
chr14:52558161
|
A | G | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+4570A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558161 | ||||||
chr14:52558201
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.444+4610G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558201 | ||||||
chr14:52558296
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+4705G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558296 | ||||||
chr14:52558305
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+4714C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558305 | ||||||
chr14:52558315
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.444+4724T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558315 | ||||||
chr14:52558409
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444+4818T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558409 | ||||||
chr14:52558446
|
A | C | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+4855A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558446 | ||||||
chr14:52558483
|
G | A | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+4892G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558483 | ||||||
chr14:52558637
|
G | C | 26 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0002g0005others(23): Show | 28 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+5046G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558637 | ||||||
chr14:52558740
|
T | A | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.444+5149T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558740 | ||||||
chr14:52558799
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444+5208A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558799 | ||||||
chr14:52558896
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.444+5305A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558896 | ||||||
chr14:52558932
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+5341A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558932 | ||||||
chr14:52559392
|
CAAAA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+5804_444+5807d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52559392 | |||||
chr14:52559403
|
C | A | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+5812C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559403 | ||||||
chr14:52559595
|
A | T | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+6004A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559595 | ||||||
chr14:52559614
|
G | A | 8 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(5): Show | 8 | HG02080.hp2 NA18945.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+6023G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559614 | ||||||
chr14:52559654
|
A | G | 7 | a0001c0006t0006g0157a0001c0006t0006g0158a0001c0006t0006g0159others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+6063A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559654 | ||||||
chr14:52559926
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+6335C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559926 | ||||||
chr14:52560161
|
A | G | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+6570A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560161 | ||||||
chr14:52560171
|
T | C | 1 | a0002c0002t0001g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.444+6580T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560171 | ||||||
chr14:52560193
|
T | A | 1 | a0001c0001t0001g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444+6602T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560193 | ||||||
chr14:52560261
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.444+6670G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560261 | ||||||
chr14:52560267
|
T | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.444+6676T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560267 | ||||||
chr14:52560426
|
G | A | 1 | a0003c0003t0001g0061 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.444+6835G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560426 | ||||||
chr14:52560440
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.444+6849G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560440 | ||||||
chr14:52560478
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.444+6887G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560478 | ||||||
chr14:52560669
|
G | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+7078G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560669 | ||||||
chr14:52560739
|
A | G | 27 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0002g0005others(24): Show | 29 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+7148A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560739 | ||||||
chr14:52560776
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+7185A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560776 | ||||||
chr14:52560817
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.444+7226G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560817 | ||||||
chr14:52560896
|
G | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+7305G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560896 | ||||||
chr14:52561030
|
A | G | 1 | a0001c0001t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.444+7439A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561030 | ||||||
chr14:52561099
|
GGTTATTA | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(81): Show | 87 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.444+7517_444+7523d others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52561099 | |||||
chr14:52561151
|
G | A | 6 | a0002c0002t0001g0012a0002c0002t0001g0062a0002c0002t0001g0063others(3): Show | 6 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+7560G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561151 | ||||||
chr14:52561190
|
C | T | 229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.444+7599C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561190 | ||||||
chr14:52561198
|
A | G | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+7607A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561198 | ||||||
chr14:52561316
|
C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+7725C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561316 | ||||||
chr14:52561334
|
G | A | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+7743G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561334 | ||||||
chr14:52561346
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+7755G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561346 | ||||||
chr14:52561382
|
A | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+7791A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561382 | ||||||
chr14:52561431
|
G | A | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.444+7840G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561431 | ||||||
chr14:52561456
|
G | A | 26 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0002g0005others(23): Show | 28 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+7865G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561456 | ||||||
chr14:52561564
|
A | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+7973A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561564 | ||||||
chr14:52561740
|
AT | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00438.hp2 HG00558.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.444+8150delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561740 | ||||||
chr14:52561768
|
A | C | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+8177A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561768 | ||||||
chr14:52561966
|
A | G | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+8375A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561966 | ||||||
chr14:52562017
|
T | G | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+8426T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562017 | ||||||
chr14:52562044
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+8453G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562044 | ||||||
chr14:52562065
|
G | A | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.444+8474G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562065 | ||||||
chr14:52562168
|
AAAAAC | A | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+8581_444+8585d others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52562168 | |||||
chr14:52562188
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+8597A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562188 | ||||||
chr14:52562403
|
A | G | 3 | a0002c0002t0001g0128a0002c0002t0001g0129a0003c0003t0002g0130 | 3 | HG00621.hp2 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.444+8812A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562403 | ||||||
chr14:52562494
|
G | A | 2 | a0003c0003t0010g0285a0003c0003t0010g0286 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+8903G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562494 | ||||||
chr14:52562517
|
G | A | 1 | a0004c0004t0001g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.444+8926G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562517 | ||||||
chr14:52562620
|
A | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+9029A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562620 | ||||||
chr14:52562835
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+9244G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562835 | ||||||
chr14:52563121
|
G | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.444+9530G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563121 | ||||||
chr14:52563358
|
TACTC | T | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+9770_444+9773d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52563358 | |||||
chr14:52563430
|
A | C | 1 | a0002c0002t0001g0288 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.444+9839A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563430 | ||||||
chr14:52563479
|
A | G | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.444+9888A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563479 | ||||||
chr14:52563601
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444+10010G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563601 | ||||||
chr14:52563647
|
A | AAC | 3 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0197 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.444+10070_444+1007 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52563647 | |||||
chr14:52563750
|
A | G | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+10159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563750 | ||||||
chr14:52563937
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444+10346T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563937 | ||||||
chr14:52563962
|
T | C | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+10371T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563962 | ||||||
chr14:52564005
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(85): Show | 91 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.444+10414G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564005 | ||||||
chr14:52564120
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+10529C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564120 | ||||||
chr14:52564269
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+10678C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564269 | ||||||
chr14:52564270
|
G | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+10679G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564270 | ||||||
chr14:52564274
|
C | CA | 127 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(124): Show | 134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.444+10701dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | |||||
chr14:52564274
|
C | CAA | 73 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0145others(70): Show | 75 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.444+10700_444+1070 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | |||||
chr14:52564274
|
C | CAAA | 10 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(7): Show | 10 | HG01261.hp1 HG02074.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+10699_444+1070 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | |||||
chr14:52564274
|
C | CAAAA | 13 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 14 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+10698_444+1070 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | |||||
chr14:52564523
|
T | C | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+10932T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564523 | ||||||
chr14:52564539
|
T | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0197 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.444+10948T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564539 | ||||||
chr14:52564552
|
A | G | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+10961A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564552 | ||||||
chr14:52564616
|
T | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+11025T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564616 | ||||||
chr14:52564643
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11052A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564643 | ||||||
chr14:52564810
|
A | C | 1 | a0001c0001t0002g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.444+11219A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564810 | ||||||
chr14:52564967
|
CA | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+11380delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564967 | |||||
chr14:52564978
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.444+11387G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564978 | ||||||
chr14:52565046
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565046 | ||||||
chr14:52565085
|
G | C | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+11494G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565085 | ||||||
chr14:52565300
|
T | C | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+11709T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565300 | ||||||
chr14:52565403
|
T | G | 1 | a0002c0002t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444+11812T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565403 | ||||||
chr14:52565575
|
C | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+11984C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565575 | ||||||
chr14:52565816
|
A | G | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+12225A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565816 | ||||||
chr14:52565860
|
T | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+12269T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565860 | ||||||
chr14:52565921
|
G | T | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+12330G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565921 | ||||||
chr14:52565941
|
G | T | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+12350G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565941 | ||||||
chr14:52566147
|
C | T | 1 | a0001c0001t0003g0323 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.444+12556C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566147 | ||||||
chr14:52566155
|
C | T | 33 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+12564C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566155 | ||||||
chr14:52566198
|
C | T | 229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.444+12607C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566198 | ||||||
chr14:52566306
|
T | G | 1 | a0001c0006t0006g0158 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.444+12715T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566306 | ||||||
chr14:52566398
|
T | G | 3 | a0001c0001t0002g0178a0001c0001t0002g0180a0001c0001t0021g0179 | 3 | HG01943.hp1 HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.444+12807T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566398 | ||||||
chr14:52566430
|
A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+12839A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566430 | ||||||
chr14:52566445
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.444+12854T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566445 | ||||||
chr14:52566544
|
T | A | 1 | a0001c0001t0015g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.444+12953T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566544 | ||||||
chr14:52566545
|
A | T | 1 | a0002c0002t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+12954A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566545 | ||||||
chr14:52566813
|
T | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+13222T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566813 | ||||||
chr14:52566833
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+13242C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566833 | ||||||
chr14:52566940
|
T | A | 2 | a0004c0004t0001g0020a0004c0004t0001g0025 | 2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.444+13349T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566940 | ||||||
chr14:52567027
|
C | T | 2 | a0004c0004t0001g0041a0004c0004t0001g0042 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.444+13436C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567027 | ||||||
chr14:52567061
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+13470C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567061 | ||||||
chr14:52567108
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+13517G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567108 | ||||||
chr14:52567279
|
T | C | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+13688T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567279 | ||||||
chr14:52567309
|
C | T | 1 | a0004c0004t0001g0273 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.444+13718C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567309 | ||||||
chr14:52567311
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444+13720C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567311 | ||||||
chr14:52567352
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.444+13761A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567352 | ||||||
chr14:52567391
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+13800A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567391 | ||||||
chr14:52567551
|
A | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.444+13960A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567551 | ||||||
chr14:52567568
|
A | G | 2 | a0001c0001t0001g0270a0004c0004t0001g0271 | 2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.444+13977A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567568 | ||||||
chr14:52567649
|
C | CT | 15 | a0001c0001t0001g0210a0001c0001t0001g0222a0001c0001t0001g0278others(12): Show | 15 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+14069dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567649 | |||||
chr14:52567649
|
CT | C | 51 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0302others(48): Show | 51 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.444+14069delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567649 | |||||
chr14:52567660
|
T | G | 2 | a0001c0001t0003g0301a0002c0002t0024g0135 | 2 | HG02074.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.444+14069T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567660 | ||||||
chr14:52567661
|
G | T | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.444+14070G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567661 | ||||||
chr14:52567662
|
G | GT | 11 | a0002c0002t0001g0068a0002c0002t0001g0073a0002c0002t0001g0119others(8): Show | 11 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+14086dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567662 | |||||
chr14:52567662
|
G | T | 1 | a0001c0001t0003g0301 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.444+14071G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567662 | ||||||
chr14:52567662
|
GT | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 51 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.444+14086delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567662 | |||||
chr14:52567663
|
T | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.444+14072T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567663 | ||||||
chr14:52567688
|
A | G | 4 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0194others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+14097A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567688 | ||||||
chr14:52567720
|
C | T | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+14129C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567720 | ||||||
chr14:52567728
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+14137C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567728 | ||||||
chr14:52567844
|
G | A | 3 | a0002c0002t0001g0074a0002c0002t0001g0075a0002c0002t0001g0076 | 3 | HG00423.hp1 HG02165.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.444+14253G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567844 | ||||||
chr14:52567879
|
C | T | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+14288C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567879 | ||||||
chr14:52567891
|
C | A | 1 | a0002c0002t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.444+14300C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567891 | ||||||
chr14:52567937
|
C | T | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+14346C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567937 | ||||||
chr14:52568209
|
A | G | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+14618A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568209 | ||||||
chr14:52568340
|
C | T | 2 | a0001c0001t0016g0192a0001c0001t0025g0193 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.444+14749C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568340 | ||||||
chr14:52568356
|
T | G | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+14765T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568356 | ||||||
chr14:52568417
|
T | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+14826T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568417 | ||||||
chr14:52568423
|
C | A | 1 | a0004c0004t0001g0268 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.444+14832C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568423 | ||||||
chr14:52568444
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.444+14853C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568444 | ||||||
chr14:52568448
|
G | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+14857G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568448 | ||||||
chr14:52568457
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.444+14866G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568457 | ||||||
chr14:52568707
|
G | A | 9 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(6): Show | 11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+15116G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568707 | ||||||
chr14:52568708
|
C | T | 9 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(6): Show | 11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+15117C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568708 | ||||||
chr14:52568839
|
C | T | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+15248C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568839 | ||||||
chr14:52568856
|
T | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.444+15265T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568856 | ||||||
chr14:52568897
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+15306G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568897 | ||||||
chr14:52568897
|
G | T | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+15306G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568897 | ||||||
chr14:52568925
|
G | A | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+15334G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568925 | ||||||
chr14:52568959
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.444+15368C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568959 | ||||||
chr14:52569022
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+15431G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569022 | ||||||
chr14:52569032
|
T | C | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+15441T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569032 | ||||||
chr14:52569083
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.444+15492G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569083 | ||||||
chr14:52569187
|
A | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+15596A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569187 | ||||||
chr14:52569190
|
G | A | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.444+15599G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569190 | ||||||
chr14:52569225
|
CAGAA | C | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+15637_444+1564 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52569225 | |||||
chr14:52569326
|
G | A | 1 | a0004c0004t0008g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.444+15735G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569326 | ||||||
chr14:52569362
|
C | CA | 21 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0223others(18): Show | 23 | HG00639.hp1 HG00733.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.444+15783dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52569362 | |||||
chr14:52569394
|
G | A | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+15803G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569394 | ||||||
chr14:52569621
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+16030C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569621 | ||||||
chr14:52569636
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+16045G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569636 | ||||||
chr14:52569651
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.444+16060G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569651 | ||||||
chr14:52569657
|
A | G | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+16066A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569657 | ||||||
chr14:52569685
|
G | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+16094G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569685 | ||||||
chr14:52569787
|
C | A | 4 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0194others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+16196C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569787 | ||||||
chr14:52569833
|
T | G | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+16242T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569833 | ||||||
chr14:52569936
|
C | T | 1 | a0004c0004t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.444+16345C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569936 | ||||||
chr14:52569939
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.444+16348G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569939 | ||||||
chr14:52570050
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+16459C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570050 | ||||||
chr14:52570082
|
G | A | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+16491G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570082 | ||||||
chr14:52570103
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+16512G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570103 | ||||||
chr14:52570316
|
A | G | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+16725A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570316 | ||||||
chr14:52570337
|
C | A | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+16746C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570337 | ||||||
chr14:52570410
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+16819C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570410 | ||||||
chr14:52570413
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(35): Show | 41 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.444+16822C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570413 | ||||||
chr14:52570436
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+16845G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570436 | ||||||
chr14:52570629
|
T | TA | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+17043dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52570629 | |||||
chr14:52570662
|
C | G | 3 | a0001c0006t0006g0158a0001c0006t0006g0159a0001c0006t0006g0163 | 3 | HG00642.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.444+17071C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570662 | ||||||
chr14:52570751
|
A | G | 3 | a0001c0006t0006g0158a0001c0006t0006g0159a0001c0006t0006g0163 | 3 | HG00642.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.444+17160A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570751 | ||||||
chr14:52570760
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.444+17169C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570760 | ||||||
chr14:52571030
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444+17439A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571030 | ||||||
chr14:52571145
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(35): Show | 41 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.444+17554C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571145 | ||||||
chr14:52571146
|
G | A | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+17555G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571146 | ||||||
chr14:52571234
|
C | T | 1 | a0003c0003t0010g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.444+17643C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571234 | ||||||
chr14:52571298
|
C | G | 173 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(170): Show | 183 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.444+17707C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571298 | ||||||
chr14:52571314
|
A | G | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+17723A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571314 | ||||||
chr14:52571459
|
A | G | 177 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(174): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.444+17868A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571459 | ||||||
chr14:52571502
|
G | A | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.444+17911G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571502 | ||||||
chr14:52571642
|
C | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0001g0255others(15): Show | 19 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.444+18051C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571642 | ||||||
chr14:52571843
|
C | T | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+18252C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571843 | ||||||
chr14:52571910
|
G | T | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.444+18319G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571910 | ||||||
chr14:52571989
|
A | C | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+18398A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571989 | ||||||
chr14:52571992
|
T | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+18401T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571992 | ||||||
chr14:52572517
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+18926T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572517 | ||||||
chr14:52572536
|
A | G | 2 | a0003c0003t0010g0285a0003c0003t0010g0286 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+18945A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572536 | ||||||
chr14:52572568
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+18977C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572568 | ||||||
chr14:52572593
|
C | A | 1 | a0001c0001t0010g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.444+19002C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572593 | ||||||
chr14:52573010
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0221a0001c0001t0001g0223others(5): Show | 9 | HG00558.hp1 HG02015.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+19419C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573010 | ||||||
chr14:52573414
|
C | T | 36 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 36 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.444+19823C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573414 | ||||||
chr14:52573415
|
G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0195 | 2 | NA20129.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.444+19824G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573415 | ||||||
chr14:52573443
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+19852G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573443 | ||||||
chr14:52573619
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+20028C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573619 | ||||||
chr14:52573634
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+20043A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573634 | ||||||
chr14:52573765
|
C | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+20174C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573765 | ||||||
chr14:52573774
|
G | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+20183G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573774 | ||||||
chr14:52573781
|
C | T | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+20190C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573781 | ||||||
chr14:52573782
|
A | G | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+20191A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573782 | ||||||
chr14:52573857
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG02145.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.444+20266G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573857 | ||||||
chr14:52573894
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+20303C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573894 | ||||||
chr14:52573957
|
CAT | C | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+20369_444+2037 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52573957 | |||||
chr14:52574003
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+20412T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574003 | ||||||
chr14:52574075
|
G | A | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+20484G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574075 | ||||||
chr14:52574096
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+20505T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574096 | ||||||
chr14:52574151
|
G | GA | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+20561dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52574151 | |||||
chr14:52574241
|
T | C | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+20650T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574241 | ||||||
chr14:52574258
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.444+20667C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574258 | ||||||
chr14:52574303
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+20712G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574303 | ||||||
chr14:52574331
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+20740A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574331 | ||||||
chr14:52574380
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444+20789A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574380 | ||||||
chr14:52574396
|
G | C | 4 | a0001c0001t0003g0302a0001c0001t0003g0303a0001c0001t0003g0313others(1): Show | 4 | HG00621.hp1 NA18969.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+20805G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574396 | ||||||
chr14:52574445
|
A | T | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+20854A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574445 | ||||||
chr14:52574488
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+20897A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574488 | ||||||
chr14:52574501
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+20910G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574501 | ||||||
chr14:52574645
|
T | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(112): Show | 123 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.444+21054T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574645 | ||||||
chr14:52574798
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+21207C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574798 | ||||||
chr14:52574831
|
T | C | 229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.444+21240T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574831 | ||||||
chr14:52575010
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+21419G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575010 | ||||||
chr14:52575102
|
G | A | 22 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(19): Show | 24 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.444+21511G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575102 | ||||||
chr14:52575128
|
A | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+21537A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575128 | ||||||
chr14:52575143
|
A | G | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+21552A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575143 | ||||||
chr14:52575149
|
C | T | 3 | a0002c0002t0001g0064a0003c0003t0010g0285a0003c0003t0010g0286 | 3 | HG00639.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+21558C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575149 | ||||||
chr14:52575200
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+21609T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575200 | ||||||
chr14:52575548
|
C | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+21957C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575548 | ||||||
chr14:52575673
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.444+22082A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575673 | ||||||
chr14:52575743
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.444+22152T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575743 | ||||||
chr14:52575915
|
G | A | 1 | a0001c0001t0003g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+22324G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575915 | ||||||
chr14:52575929
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+22338A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575929 | ||||||
chr14:52576088
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-22184C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576088 | ||||||
chr14:52576163
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-22109C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576163 | ||||||
chr14:52576182
|
A | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-22090A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576182 | ||||||
chr14:52576197
|
C | T | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-22075C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576197 | ||||||
chr14:52576437
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.445-21835G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576437 | ||||||
chr14:52576509
|
T | C | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-21763T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576509 | ||||||
chr14:52576546
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445-21726T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576546 | ||||||
chr14:52576632
|
C | G | 1 | a0007c0010t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445-21640C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576632 | ||||||
chr14:52576792
|
C | T | 1 | a0004c0004t0001g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.445-21480C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576792 | ||||||
chr14:52576956
|
G | A | 1 | a0001c0001t0003g0305 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.445-21316G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576956 | ||||||
chr14:52576960
|
C | T | 1 | a0006c0008t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.445-21312C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576960 | ||||||
chr14:52576963
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-21309G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576963 | ||||||
chr14:52577056
|
G | GGTGCACA others(1): Show |
229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.445-21216_445-2121 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577056 | ||||||
chr14:52577068
|
GCTACT | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-21197_445-2119 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577068 | |||||
chr14:52577123
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-21149G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577123 | ||||||
chr14:52577134
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445-21138C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577134 | ||||||
chr14:52577166
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0169others(12): Show | 17 | HG00558.hp1 HG01074.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.445-21106G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577166 | ||||||
chr14:52577183
|
C | CA | 29 | a0001c0001t0001g0080a0001c0001t0003g0299a0001c0001t0003g0300others(26): Show | 29 | HG00642.hp2 HG00673.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-21059dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
C | CAA | 7 | a0001c0001t0003g0317a0001c0001t0003g0318a0001c0001t0003g0323others(4): Show | 7 | HG03579.hp1 NA18953.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-21060_445-2105 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
C | CAAAAAA | 6 | a0003c0003t0009g0047a0003c0003t0009g0048a0003c0003t0011g0282others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-21064_445-2105 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.445-21089C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577183 | ||||||
chr14:52577183
|
CA | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0171a0001c0001t0002g0005others(35): Show | 41 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.445-21059delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAA | C | 28 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(25): Show | 28 | HG01167.hp1 HG01261.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.445-21060_445-2105 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAAA | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 59 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.445-21061_445-2105 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAAAA | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 11 | HG00099.hp2 HG00738.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21062_445-2105 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAAAAA | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 41 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.445-21063_445-2105 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAAAAAA | C | 12 | a0001c0005t0005g0204a0001c0005t0007g0003a0001c0005t0007g0296others(9): Show | 14 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-21064_445-2105 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577183
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.445-21069_445-2105 others(15): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | |||||
chr14:52577221
|
G | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-21051G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577221 | ||||||
chr14:52577383
|
A | C | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-20889A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577383 | ||||||
chr14:52577385
|
T | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(174): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.445-20887T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577385 | ||||||
chr14:52577505
|
T | TGC | 7 | a0001c0001t0003g0299a0001c0001t0003g0305a0001c0001t0003g0312others(4): Show | 7 | HG01099.hp1 NA18960.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-20756_445-2075 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577505 | |||||
chr14:52577507
|
C | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 93 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.445-20765C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577507 | ||||||
chr14:52577512
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-20760G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577512 | ||||||
chr14:52577514
|
G | GCACACAC others(1): Show |
6 | a0001c0001t0002g0005a0001c0001t0002g0177a0001c0001t0002g0191others(3): Show | 7 | HG00280.hp1 HG01069.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACACAC others(3): Show |
12 | a0001c0001t0002g0049a0001c0001t0002g0176a0001c0001t0002g0180others(9): Show | 12 | HG01192.hp2 HG01884.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.445-20757_445-2075 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACACAC others(7): Show |
3 | a0001c0001t0001g0030a0001c0001t0002g0178a0001c0001t0002g0186 | 3 | HG00733.hp1 HG02004.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.445-20757_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACACAC others(13): Show |
1 | a0001c0001t0002g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.445-20757_445-2075 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACGCAC others(7): Show |
6 | a0001c0001t0001g0021a0004c0004t0001g0013a0004c0004t0001g0020others(3): Show | 6 | HG01496.hp1 HG01993.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577514
|
G | GCACGCAC others(9): Show |
3 | a0001c0001t0001g0032a0001c0001t0002g0024a0001c0001t0002g0031 | 3 | NA18952.hp1 NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.445-20757_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | |||||
chr14:52577516
|
G | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0032others(29): Show | 33 | HG00280.hp1 HG00733.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.445-20756G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577516 | ||||||
chr14:52577516
|
G | GCA | 20 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(17): Show | 20 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-20732_445-2073 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACA | 3 | a0001c0001t0013g0167a0002c0002t0012g0050a0006c0008t0001g0173 | 3 | HG01074.hp2 HG02886.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.445-20734_445-2073 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACACA | 10 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0209others(7): Show | 13 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-20736_445-2073 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACACAC others(1): Show |
5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-20738_445-2073 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.445-20740_445-2073 others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0145 | 3 | HG00438.hp2 HG02976.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.445-20742_445-2073 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCACACAC others(13): Show |
1 | a0001c0001t0002g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.445-20750_445-2073 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(7): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0019g0038others(1): Show | 4 | HG00558.hp2 NA18975.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(9): Show |
9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(6): Show | 9 | HG01978.hp1 HG02071.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(11): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0043others(1): Show | 4 | HG00735.hp1 HG02155.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(22): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(13): Show |
1 | a0001c0001t0001g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445-20755_445-2075 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCACAC others(17): Show |
1 | a0004c0004t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(28): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCGCAC others(9): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0029 | 2 | HG02055.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.445-20755_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
G | GCGCGCAC others(11): Show |
1 | a0004c0004t0001g0023 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(22): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
GCA | G | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 86 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.445-20732_445-2073 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577516
|
GCACA | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0247a0003c0003t0011g0282others(3): Show | 6 | HG02717.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-20734_445-2073 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | |||||
chr14:52577518
|
A | G | 42 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0302others(39): Show | 42 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.445-20754A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577518 | ||||||
chr14:52577556
|
A | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-20716A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577556 | ||||||
chr14:52577592
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-20680G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577592 | ||||||
chr14:52577598
|
CAAAAG | C | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.445-20671_445-2066 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577598 | |||||
chr14:52577701
|
G | A | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.445-20571G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577701 | ||||||
chr14:52577743
|
G | T | 1 | a0001c0001t0001g0290 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.445-20529G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577743 | ||||||
chr14:52577798
|
A | C | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.445-20474A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577798 | ||||||
chr14:52577799
|
C | CA | 103 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0164others(100): Show | 106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.445-20455dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | |||||
chr14:52577799
|
C | CAAAA | 25 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0026others(22): Show | 25 | HG00733.hp1 HG00735.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.445-20458_445-2045 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | |||||
chr14:52577799
|
C | CAAAAA | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 10 | HG00438.hp2 HG00558.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-20459_445-2045 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | |||||
chr14:52577881
|
C | G | 8 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0138others(5): Show | 8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-20391C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577881 | ||||||
chr14:52577895
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.445-20377G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577895 | ||||||
chr14:52577897
|
A | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-20375A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577897 | ||||||
chr14:52578191
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-20081A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578191 | ||||||
chr14:52578238
|
A | T | 18 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(15): Show | 18 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.445-20034A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578238 | ||||||
chr14:52578266
|
C | T | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.445-20006C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578266 | ||||||
chr14:52578360
|
G | A | 2 | a0004c0004t0001g0041a0004c0004t0001g0042 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.445-19912G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578360 | ||||||
chr14:52578366
|
T | A | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-19906T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578366 | ||||||
chr14:52578429
|
A | G | 1 | a0001c0001t0003g0300 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.445-19843A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578429 | ||||||
chr14:52578490
|
C | G | 1 | a0002c0002t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.445-19782C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578490 | ||||||
chr14:52578658
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-19614A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578658 | ||||||
chr14:52578660
|
G | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-19612G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578660 | ||||||
chr14:52578661
|
C | A | 14 | a0001c0001t0003g0314a0001c0001t0003g0317a0001c0001t0003g0318others(11): Show | 14 | HG01099.hp1 NA18939.hp2 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-19611C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578661 | ||||||
chr14:52578770
|
C | T | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-19502C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578770 | ||||||
chr14:52578883
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-19389G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578883 | ||||||
chr14:52579046
|
C | T | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-19226C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579046 | ||||||
chr14:52579055
|
T | C | 1 | a0004c0004t0008g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.445-19217T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579055 | ||||||
chr14:52579131
|
A | C | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.445-19141A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579131 | ||||||
chr14:52579137
|
C | G | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445-19135C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579137 | ||||||
chr14:52579143
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.445-19129C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579143 | ||||||
chr14:52579182
|
G | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.445-19090G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579182 | ||||||
chr14:52579304
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0292others(1): Show | 4 | NA18959.hp2 NA18993.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-18968C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579304 | ||||||
chr14:52579358
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.445-18914G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579358 | ||||||
chr14:52579514
|
A | G | 1 | a0004c0004t0001g0013 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.445-18758A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579514 | ||||||
chr14:52579526
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-18746T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579526 | ||||||
chr14:52579650
|
A | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 229 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.445-18622A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579650 | ||||||
chr14:52579789
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-18483G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579789 | ||||||
chr14:52579841
|
G | A | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-18431G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579841 | ||||||
chr14:52579883
|
G | A | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-18389G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579883 | ||||||
chr14:52579918
|
T | C | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-18354T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579918 | ||||||
chr14:52580011
|
A | G | 1 | a0004c0004t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.445-18261A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580011 | ||||||
chr14:52580113
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-18159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580113 | ||||||
chr14:52580177
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.445-18095A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580177 | ||||||
chr14:52580277
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-17995G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580277 | ||||||
chr14:52580361
|
G | GA | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(85): Show | 93 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.445-17902dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580361 | |||||
chr14:52580370
|
AT | A | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-17892delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580370 | |||||
chr14:52580529
|
T | A | 1 | a0004c0004t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.445-17743T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580529 | ||||||
chr14:52580584
|
G | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.445-17688G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580584 | ||||||
chr14:52580634
|
G | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-17638G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580634 | ||||||
chr14:52580807
|
ATTAT | A | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-17460_445-1745 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580807 | |||||
chr14:52580811
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-17461T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580811 | ||||||
chr14:52580831
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-17441T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580831 | ||||||
chr14:52580868
|
T | G | 1 | a0001c0001t0001g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.445-17404T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580868 | ||||||
chr14:52580874
|
G | A | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.445-17398G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580874 | ||||||
chr14:52580909
|
A | T | 1 | a0001c0001t0003g0321 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.445-17363A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580909 | ||||||
chr14:52581144
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-17128C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581144 | ||||||
chr14:52581195
|
C | CA | 39 | a0001c0001t0001g0223a0001c0001t0002g0005a0001c0001t0002g0006others(36): Show | 43 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.445-17059dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581195 | |||||
chr14:52581195
|
CA | C | 12 | a0001c0001t0001g0182a0001c0001t0001g0245a0001c0001t0001g0256others(9): Show | 12 | HG00738.hp1 HG01167.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-17059delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581195 | |||||
chr14:52581230
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.445-17042T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581230 | ||||||
chr14:52581245
|
A | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-17027A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581245 | ||||||
chr14:52581247
|
C | T | 1 | a0002c0002t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.445-17025C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581247 | ||||||
chr14:52581290
|
C | T | 221 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.445-16982C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581290 | ||||||
chr14:52581370
|
TA | T | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.445-16885delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581370 | |||||
chr14:52581533
|
C | CA | 47 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 48 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.445-16726dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581533 | |||||
chr14:52581622
|
T | A | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16650T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581622 | ||||||
chr14:52581631
|
A | G | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-16641A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581631 | ||||||
chr14:52581669
|
A | G | 2 | a0003c0003t0010g0285a0003c0003t0010g0286 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.445-16603A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581669 | ||||||
chr14:52581696
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.445-16576A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581696 | ||||||
chr14:52581814
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16458T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581814 | ||||||
chr14:52581976
|
G | A | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-16296G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581976 | ||||||
chr14:52582060
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-16212T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582060 | ||||||
chr14:52582130
|
C | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16142C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582130 | ||||||
chr14:52582796
|
AAAAT | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-15465_445-1546 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52582796 | |||||
chr14:52582935
|
A | G | 1 | a0005c0009t0001g0269 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.445-15337A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582935 | ||||||
chr14:52583170
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-15102A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583170 | ||||||
chr14:52583206
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-15066G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583206 | ||||||
chr14:52583551
|
G | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(214): Show | 227 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.445-14721G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583551 | ||||||
chr14:52583611
|
C | T | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-14661C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583611 | ||||||
chr14:52583736
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445-14536C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583736 | ||||||
chr14:52583773
|
C | CAGA | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-14499_445-1449 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583773 | ||||||
chr14:52583774
|
T | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-14498T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583774 | ||||||
chr14:52583807
|
A | C | 1 | a0003c0003t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.445-14465A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583807 | ||||||
chr14:52583898
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.445-14374A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583898 | ||||||
chr14:52583928
|
CTG | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-14343_445-1434 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583928 | ||||||
chr14:52584214
|
A | G | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-14058A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584214 | ||||||
chr14:52584359
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-13913A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584359 | ||||||
chr14:52584476
|
A | G | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-13796A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584476 | ||||||
chr14:52584643
|
G | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-13629G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584643 | ||||||
chr14:52584748
|
C | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-13524C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584748 | ||||||
chr14:52584832
|
C | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0187a0001c0001t0002g0188 | 3 | NA18968.hp1 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.445-13440C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584832 | ||||||
chr14:52584859
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.445-13413C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584859 | ||||||
chr14:52584944
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-13328A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584944 | ||||||
chr14:52585011
|
C | T | 1 | a0002c0002t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-13261C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585011 | ||||||
chr14:52585079
|
T | C | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445-13193T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585079 | ||||||
chr14:52585154
|
G | A | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.445-13118G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585154 | ||||||
chr14:52585301
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-12971T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585301 | ||||||
chr14:52585379
|
G | GCT | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-12883_445-1288 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52585379 | |||||
chr14:52585449
|
A | G | 1 | a0001c0001t0002g0180 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.445-12823A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585449 | ||||||
chr14:52585508
|
A | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.445-12764A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585508 | ||||||
chr14:52585671
|
T | TA | 15 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 16 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.445-12595dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52585671 | |||||
chr14:52585741
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-12531G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585741 | ||||||
chr14:52585994
|
G | A | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-12278G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585994 | ||||||
chr14:52586069
|
G | A | 32 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(29): Show | 32 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.445-12203G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586069 | ||||||
chr14:52586120
|
A | G | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.445-12152A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586120 | ||||||
chr14:52586411
|
A | G | 1 | a0001c0001t0002g0186 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445-11861A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586411 | ||||||
chr14:52586506
|
A | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0153 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.445-11766A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586506 | ||||||
chr14:52586623
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-11649A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586623 | ||||||
chr14:52586670
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.445-11602C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586670 | ||||||
chr14:52586757
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.445-11515T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586757 | ||||||
chr14:52586772
|
T | A | 18 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(15): Show | 20 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-11500T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586772 | ||||||
chr14:52586813
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-11459C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586813 | ||||||
chr14:52587110
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.445-11162G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587110 | ||||||
chr14:52587121
|
C | A | 6 | a0003c0003t0001g0067a0003c0003t0001g0103a0003c0003t0001g0104others(3): Show | 6 | HG01433.hp1 HG02145.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-11151C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587121 | ||||||
chr14:52587182
|
G | A | 1 | a0002c0002t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.445-11090G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587182 | ||||||
chr14:52587208
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-11064A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587208 | ||||||
chr14:52587212
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-11060G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587212 | ||||||
chr14:52587262
|
T | C | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-11010T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587262 | ||||||
chr14:52587546
|
A | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-10726A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587546 | ||||||
chr14:52587795
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-10477C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587795 | ||||||
chr14:52587844
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-10428A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587844 | ||||||
chr14:52587921
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-10351C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587921 | ||||||
chr14:52588099
|
G | A | 7 | a0001c0006t0006g0157a0001c0006t0006g0158a0001c0006t0006g0159others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-10173G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588099 | ||||||
chr14:52588227
|
C | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-10045C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588227 | ||||||
chr14:52588247
|
C | G | 1 | a0001c0001t0004g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445-10025C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588247 | ||||||
chr14:52588334
|
A | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(131): Show | 141 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.445-9938A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588334 | ||||||
chr14:52588461
|
A | G | 1 | a0001c0001t0010g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445-9811A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588461 | ||||||
chr14:52588640
|
A | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-9632A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588640 | ||||||
chr14:52588678
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-9594A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588678 | ||||||
chr14:52588760
|
G | A | 1 | a0002c0002t0001g0136 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.445-9512G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588760 | ||||||
chr14:52588818
|
G | T | 1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.445-9454G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588818 | ||||||
chr14:52588855
|
T | C | 1 | a0001c0001t0002g0005 | 2 | HG00280.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.445-9417T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588855 | ||||||
chr14:52588945
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0264 | 3 | HG00423.hp2 HG00609.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.445-9327C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588945 | ||||||
chr14:52588946
|
G | A | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-9326G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588946 | ||||||
chr14:52589454
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.445-8818A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589454 | ||||||
chr14:52589810
|
G | A | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-8462G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589810 | ||||||
chr14:52589889
|
T | C | 22 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(19): Show | 24 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.445-8383T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589889 | ||||||
chr14:52590062
|
T | C | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-8210T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590062 | ||||||
chr14:52590253
|
GA | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-8010delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52590253 | |||||
chr14:52590263
|
G | T | 1 | a0004c0004t0001g0268 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.445-8009G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590263 | ||||||
chr14:52590265
|
T | G | 1 | a0001c0001t0004g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.445-8007T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590265 | ||||||
chr14:52590387
|
T | C | 6 | a0001c0001t0003g0299a0001c0001t0003g0302a0001c0001t0003g0303others(3): Show | 6 | HG00621.hp1 NA18969.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7885T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590387 | ||||||
chr14:52590444
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-7828G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590444 | ||||||
chr14:52590738
|
T | C | 2 | a0002c0002t0001g0083a0002c0002t0001g0106 | 2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.445-7534T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590738 | ||||||
chr14:52590789
|
T | G | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-7483T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590789 | ||||||
chr14:52590990
|
C | A | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-7282C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590990 | ||||||
chr14:52591034
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-7238A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591034 | ||||||
chr14:52591095
|
C | T | 5 | a0004c0004t0001g0198a0004c0004t0001g0246a0004c0004t0001g0268others(2): Show | 5 | HG02015.hp1 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-7177C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591095 | ||||||
chr14:52591536
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-6736G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591536 | ||||||
chr14:52591981
|
C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-6291C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591981 | ||||||
chr14:52592012
|
C | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-6260C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592012 | ||||||
chr14:52592239
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-6033A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592239 | ||||||
chr14:52592274
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-5998G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592274 | ||||||
chr14:52592278
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-5994T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592278 | ||||||
chr14:52592392
|
A | T | 1 | a0002c0002t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445-5880A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592392 | ||||||
chr14:52592415
|
C | G | 1 | a0001c0001t0002g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.445-5857C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592415 | ||||||
chr14:52592937
|
T | C | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-5335T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592937 | ||||||
chr14:52593036
|
A | G | 17 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(14): Show | 19 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.445-5236A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593036 | ||||||
chr14:52593059
|
G | A | 2 | a0001c0001t0001g0043a0004c0004t0001g0023 | 2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.445-5213G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593059 | ||||||
chr14:52593160
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-5112C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593160 | ||||||
chr14:52593260
|
T | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-5012T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593260 | ||||||
chr14:52593289
|
T | G | 2 | a0002c0002t0001g0092a0002c0002t0001g0120 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.445-4983T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593289 | ||||||
chr14:52593380
|
T | G | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(21): Show | 26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-4892T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593380 | ||||||
chr14:52593528
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-4744G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593528 | ||||||
chr14:52593662
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.445-4610G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593662 | ||||||
chr14:52593745
|
C | T | 22 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(19): Show | 24 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.445-4527C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593745 | ||||||
chr14:52593777
|
C | T | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.445-4495C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593777 | ||||||
chr14:52593796
|
AT | A | 325 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.445-4469delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52593796 | |||||
chr14:52593913
|
T | C | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-4359T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593913 | ||||||
chr14:52594174
|
C | CTG | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-4095_445-4094d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52594174 | |||||
chr14:52594301
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-3971T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594301 | ||||||
chr14:52594335
|
T | A | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.445-3937T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594335 | ||||||
chr14:52594394
|
T | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0164others(82): Show | 88 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.445-3878T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594394 | ||||||
chr14:52594683
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-3589C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594683 | ||||||
chr14:52594700
|
T | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.445-3572T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594700 | ||||||
chr14:52594787
|
T | C | 5 | a0002c0002t0001g0119a0002c0002t0001g0121a0002c0002t0001g0126others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-3485T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594787 | ||||||
chr14:52594957
|
C | T | 45 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(42): Show | 45 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.445-3315C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594957 | ||||||
chr14:52595152
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-3120C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595152 | ||||||
chr14:52595177
|
C | T | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-3095C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595177 | ||||||
chr14:52595335
|
T | C | 1 | a0002c0002t0001g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.445-2937T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595335 | ||||||
chr14:52595405
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-2867A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595405 | ||||||
chr14:52595438
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-2834A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595438 | ||||||
chr14:52595525
|
T | G | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-2747T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595525 | ||||||
chr14:52595609
|
C | T | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445-2663C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595609 | ||||||
chr14:52595651
|
A | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.445-2621A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595651 | ||||||
chr14:52595716
|
G | A | 1 | a0001c0001t0003g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445-2556G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595716 | ||||||
chr14:52595817
|
G | A | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-2455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595817 | ||||||
chr14:52595842
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-2430T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595842 | ||||||
chr14:52595895
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0264 | 3 | HG00423.hp2 HG00609.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.445-2377G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595895 | ||||||
chr14:52595902
|
G | C | 8 | a0002c0002t0001g0287a0002c0002t0001g0288a0003c0003t0010g0285others(5): Show | 8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-2370G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595902 | ||||||
chr14:52595997
|
G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2275G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595997 | ||||||
chr14:52596181
|
C | T | 2 | a0001c0001t0004g0151a0001c0001t0004g0154 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.445-2091C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596181 | ||||||
chr14:52596197
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-2075C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596197 | ||||||
chr14:52596235
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-2037G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596235 | ||||||
chr14:52596269
|
CACGGGTC others(21): Show |
C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-2002_445-1975d others(30): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596269 | ||||||
chr14:52596317
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1955T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596317 | ||||||
chr14:52596329
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1943C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596329 | ||||||
chr14:52596352
|
C | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1920C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596352 | ||||||
chr14:52596354
|
A | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1918A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596354 | ||||||
chr14:52596357
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1915T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596357 | ||||||
chr14:52596358
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1914G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596358 | ||||||
chr14:52596360
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1912T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596360 | ||||||
chr14:52596361
|
A | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1911A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596361 | ||||||
chr14:52596374
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1898T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596374 | ||||||
chr14:52596378
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1894T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596378 | ||||||
chr14:52596390
|
G | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1882G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596390 | ||||||
chr14:52596441
|
G | A | 2 | a0001c0001t0016g0192a0001c0001t0025g0193 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445-1831G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596441 | ||||||
chr14:52596446
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-1826G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596446 | ||||||
chr14:52596452
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-1820C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596452 | ||||||
chr14:52596545
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-1727C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596545 | ||||||
chr14:52596664
|
C | G | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445-1608C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596664 | ||||||
chr14:52596730
|
C | T | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-1542C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596730 | ||||||
chr14:52596895
|
T | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-1377T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596895 | ||||||
chr14:52596903
|
G | A | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(96): Show | 106 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.445-1369G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596903 | ||||||
chr14:52597032
|
C | T | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445-1240C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597032 | ||||||
chr14:52597169
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-1103G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597169 | ||||||
chr14:52597189
|
C | T | 2 | a0004c0004t0001g0041a0004c0004t0001g0042 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.445-1083C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597189 | ||||||
chr14:52597321
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.445-951C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597321 | ||||||
chr14:52597465
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.445-807C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597465 | ||||||
chr14:52597563
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-709G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597563 | ||||||
chr14:52597681
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.445-591T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597681 | ||||||
chr14:52597737
|
T | G | 2 | a0001c0001t0016g0192a0001c0001t0025g0193 | 2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445-535T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597737 | ||||||
chr14:52597845
|
A | T | 229 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.445-427A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597845 | ||||||
chr14:52597971
|
C | T | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-301C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597971 | ||||||
chr14:52598070
|
G | A | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445-202G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52598070 | ||||||
chr14:52598170
|
A | G | 1 | a0001c0001t0003g0307 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.445-102A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52598170 | ||||||
chr14:52598387
|
T | A | 9 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(6): Show | 11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+72T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598387 | ||||||
chr14:52598425
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+110C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598425 | ||||||
chr14:52598454
|
A | G | 2 | a0001c0005t0005g0008a0001c0005t0005g0200 | 3 | HG00738.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.488+139A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598454 | ||||||
chr14:52598542
|
C | A | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.488+227C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598542 | ||||||
chr14:52598762
|
C | G | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488+447C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598762 | ||||||
chr14:52598767
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.488+452T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598767 | ||||||
chr14:52598808
|
A | T | 2 | a0001c0001t0001g0043a0004c0004t0001g0023 | 2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.488+493A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598808 | ||||||
chr14:52598996
|
C | T | 59 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(56): Show | 61 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.488+681C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598996 | ||||||
chr14:52599171
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+856C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599171 | ||||||
chr14:52599218
|
G | C | 2 | a0001c0001t0001g0218a0001c0001t0015g0217 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489-895G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599218 | ||||||
chr14:52599228
|
T | A | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.489-885T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599228 | ||||||
chr14:52599250
|
G | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(33): Show | 39 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.489-863G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599250 | ||||||
chr14:52599317
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489-796A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599317 | ||||||
chr14:52599434
|
C | CT | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.489-663dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | |||||
chr14:52599434
|
CT | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.489-663delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | |||||
chr14:52599434
|
CTT | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489-664_489-663del others(2): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | |||||
chr14:52599450
|
T | A | 1 | a0004c0004t0001g0246 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.489-663T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599450 | ||||||
chr14:52599464
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.489-649C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599464 | ||||||
chr14:52599465
|
G | A | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(22): Show | 27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.489-648G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599465 | ||||||
chr14:52599500
|
C | T | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-613C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599500 | ||||||
chr14:52599579
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489-534G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599579 | ||||||
chr14:52599673
|
A | T | 2 | a0002c0002t0001g0088a0002c0002t0001g0113 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.489-440A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599673 | ||||||
chr14:52599686
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489-427G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599686 | ||||||
chr14:52599774
|
C | T | 44 | a0001c0001t0003g0299a0001c0001t0003g0300a0001c0001t0003g0301others(41): Show | 44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.489-339C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599774 | ||||||
chr14:52599795
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489-318A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599795 | ||||||
chr14:52599827
|
A | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.489-286A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599827 | ||||||
chr14:52599833
|
C | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-280C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599833 | ||||||
chr14:52599881
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.489-232A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599881 | ||||||
chr14:52600428
|
C | CTATTT | 12 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(9): Show | 13 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+113_717+117dup others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | |||||
chr14:52600428
|
C | CTATTTTA others(3): Show |
1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.717+108_717+117dup others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | |||||
chr14:52600428
|
CTATTT | C | 87 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(84): Show | 92 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.717+113_717+117del others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | |||||
chr14:52600617
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.717+276T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600617 | ||||||
chr14:52600868
|
A | G | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.717+527A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600868 | ||||||
chr14:52600963
|
G | A | 241 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(238): Show | 251 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.717+622G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600963 | ||||||
chr14:52601005
|
G | T | 8 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+664G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601005 | ||||||
chr14:52601035
|
A | G | 1 | a0003c0003t0010g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.717+694A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601035 | ||||||
chr14:52601042
|
A | G | 1 | a0001c0006t0006g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.717+701A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601042 | ||||||
chr14:52601283
|
G | A | 2 | a0001c0001t0014g0235a0001c0001t0014g0236 | 2 | HG00639.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.717+942G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601283 | ||||||
chr14:52601439
|
T | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+1098T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601439 | ||||||
chr14:52601466
|
G | A | 2 | a0001c0006t0006g0157a0001c0006t0006g0160 | 2 | HG00735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.717+1125G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601466 | ||||||
chr14:52601478
|
A | ATG | 8 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0138others(5): Show | 8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.717+1157_717+1158d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | |||||
chr14:52601478
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(7): Show | 11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.717+1137A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601478 | ||||||
chr14:52601478
|
ATG | A | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.717+1157_717+1158d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | |||||
chr14:52601478
|
ATGTG | A | 20 | a0001c0001t0001g0199a0001c0005t0005g0007a0001c0005t0005g0008others(17): Show | 24 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.717+1155_717+1158d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | |||||
chr14:52601478
|
ATGTGTG | A | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.717+1153_717+1158d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | |||||
chr14:52601498
|
G | A | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.717+1157G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601498 | ||||||
chr14:52601498
|
G | GTA | 13 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 14 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.717+1168_717+1169d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601498 | |||||
chr14:52601500
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.717+1159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601500 | ||||||
chr14:52601509
|
T | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.717+1168T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601509 | ||||||
chr14:52601511
|
G | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 46 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.717+1170G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601511 | ||||||
chr14:52601546
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.717+1205T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601546 | ||||||
chr14:52601563
|
T | C | 1 | a0002c0002t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.717+1222T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601563 | ||||||
chr14:52601664
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+1323T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601664 | ||||||
chr14:52601741
|
A | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1400A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601741 | ||||||
chr14:52601809
|
C | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0153 | 2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.717+1468C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601809 | ||||||
chr14:52601811
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1470A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601811 | ||||||
chr14:52601871
|
A | C | 11 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(8): Show | 13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+1530A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601871 | ||||||
chr14:52602204
|
T | C | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.717+1863T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602204 | ||||||
chr14:52602359
|
C | T | 2 | a0002c0002t0001g0140a0002c0002t0001g0142 | 2 | NA18970.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.717+2018C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602359 | ||||||
chr14:52602366
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+2025A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602366 | ||||||
chr14:52602625
|
G | T | 1 | a0002c0002t0001g0075 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.717+2284G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602625 | ||||||
chr14:52602729
|
A | G | 2 | a0002c0002t0001g0083a0002c0002t0001g0106 | 2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.717+2388A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602729 | ||||||
chr14:52602733
|
G | A | 12 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(9): Show | 14 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.717+2392G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602733 | ||||||
chr14:52602774
|
T | C | 74 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 77 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.717+2433T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602774 | ||||||
chr14:52602796
|
T | G | 5 | a0001c0001t0001g0080a0002c0002t0001g0116a0002c0002t0001g0124others(2): Show | 5 | HG00323.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+2455T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602796 | ||||||
chr14:52602946
|
A | G | 1 | a0001c0001t0019g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.717+2605A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602946 | ||||||
chr14:52603460
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.717+3119C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603460 | ||||||
chr14:52603496
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.717+3155T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603496 | ||||||
chr14:52603531
|
T | C | 1 | a0003c0003t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.717+3190T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603531 | ||||||
chr14:52603608
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+3267C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603608 | ||||||
chr14:52603609
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0015g0217others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+3268G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603609 | ||||||
chr14:52603660
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.717+3319G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603660 | ||||||
chr14:52603747
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+3406C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603747 | ||||||
chr14:52603857
|
C | T | 1 | a0002c0002t0018g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+3516C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603857 | ||||||
chr14:52603888
|
T | A | 1 | a0001c0001t0013g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.717+3547T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603888 | ||||||
chr14:52604598
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+4257A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604598 | ||||||
chr14:52604647
|
C | T | 7 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(4): Show | 9 | HG00609.hp1 HG00738.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+4306C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604647 | ||||||
chr14:52604742
|
A | G | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+4401A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604742 | ||||||
chr14:52604997
|
C | T | 322 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.717+4656C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604997 | ||||||
chr14:52605184
|
G | A | 318 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(315): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.717+4843G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605184 | ||||||
chr14:52605226
|
TTC | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0015g0217others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+4887_717+4888d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52605226 | |||||
chr14:52605247
|
G | T | 30 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 30 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+4906G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605247 | ||||||
chr14:52605572
|
T | A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5231T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605572 | ||||||
chr14:52605610
|
T | C | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5269T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605610 | ||||||
chr14:52605632
|
A | G | 2 | a0002c0002t0001g0287a0002c0002t0001g0288 | 2 | HG01496.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.717+5291A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605632 | ||||||
chr14:52605737
|
C | T | 17 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(14): Show | 19 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.717+5396C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605737 | ||||||
chr14:52606274
|
A | G | 2 | a0001c0001t0001g0209a0003c0003t0001g0143 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.717+5933A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606274 | ||||||
chr14:52606332
|
G | A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5991G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606332 | ||||||
chr14:52606676
|
A | G | 2 | a0001c0001t0002g0194a0008c0011t0002g0174 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.717+6335A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606676 | ||||||
chr14:52606685
|
A | T | 2 | a0001c0001t0001g0045a0001c0005t0017g0293 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.717+6344A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606685 | ||||||
chr14:52606903
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0272 | 2 | NA18965.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.717+6562A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606903 | ||||||
chr14:52606917
|
G | A | 1 | a0002c0002t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.717+6576G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606917 | ||||||
chr14:52607063
|
T | C | 2 | a0001c0001t0014g0235a0001c0001t0014g0236 | 2 | HG00639.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.717+6722T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607063 | ||||||
chr14:52607210
|
G | A | 312 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(309): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.717+6869G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607210 | ||||||
chr14:52607421
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+7080A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607421 | ||||||
chr14:52607695
|
CA | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0216a0001c0001t0001g0243others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.717+7358delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52607695 | |||||
chr14:52607874
|
C | CA | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+7546dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52607874 | |||||
chr14:52607996
|
G | T | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 50 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.717+7655G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607996 | ||||||
chr14:52608138
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+7797C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608138 | ||||||
chr14:52608273
|
T | A | 1 | a0001c0005t0005g0202 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.717+7932T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608273 | ||||||
chr14:52608430
|
G | T | 152 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0021others(149): Show | 158 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.717+8089G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608430 | ||||||
chr14:52608690
|
G | T | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+8349G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608690 | ||||||
chr14:52608714
|
C | CT | 8 | a0001c0001t0001g0226a0001c0001t0021g0179a0003c0003t0010g0285others(5): Show | 8 | HG01978.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+8384dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52608714 | |||||
chr14:52608761
|
C | G | 2 | a0003c0003t0010g0285a0003c0003t0010g0286 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+8420C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608761 | ||||||
chr14:52608878
|
G | C | 2 | a0003c0003t0010g0285a0003c0003t0010g0286 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+8537G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608878 | ||||||
chr14:52608982
|
G | A | 2 | a0002c0002t0001g0125a0002c0002t0018g0081 | 2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.717+8641G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608982 | ||||||
chr14:52609336
|
A | G | 1 | a0001c0001t0003g0327 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.717+8995A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609336 | ||||||
chr14:52609673
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9332C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609673 | ||||||
chr14:52609674
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.717+9333G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609674 | ||||||
chr14:52609700
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+9359G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609700 | ||||||
chr14:52609732
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.717+9391G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609732 | ||||||
chr14:52609743
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0171others(3): Show | 7 | HG01074.hp2 HG02451.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+9402G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609743 | ||||||
chr14:52609752
|
G | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9411G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609752 | ||||||
chr14:52609796
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.717+9455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609796 | ||||||
chr14:52609796
|
G | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9455G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609796 | ||||||
chr14:52610018
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+9677A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610018 | ||||||
chr14:52610029
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+9688C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610029 | ||||||
chr14:52610091
|
A | G | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+9750A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610091 | ||||||
chr14:52610094
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+9753C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610094 | ||||||
chr14:52610276
|
C | G | 1 | a0002c0002t0001g0129 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.717+9935C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610276 | ||||||
chr14:52610385
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+10044G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610385 | ||||||
chr14:52610406
|
C | A | 1 | a0002c0002t0001g0137 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.717+10065C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610406 | ||||||
chr14:52610425
|
G | GAGTAC | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.717+10091_717+1009 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52610425 | |||||
chr14:52610535
|
G | C | 318 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(315): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.717+10194G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610535 | ||||||
chr14:52610568
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.717+10227G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610568 | ||||||
chr14:52610603
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+10262G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610603 | ||||||
chr14:52610624
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+10283T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610624 | ||||||
chr14:52610640
|
G | A | 7 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0088others(4): Show | 7 | HG00323.hp2 HG00642.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+10299G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610640 | ||||||
chr14:52611307
|
A | G | 1 | a0001c0001t0008g0304 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.717+10966A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611307 | ||||||
chr14:52611314
|
T | C | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+10973T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611314 | ||||||
chr14:52611340
|
A | G | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+10999A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611340 | ||||||
chr14:52611354
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.717+11013C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611354 | ||||||
chr14:52611379
|
T | C | 1 | a0004c0004t0001g0022 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.717+11038T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611379 | ||||||
chr14:52611768
|
A | C | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.717+11427A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611768 | ||||||
chr14:52611880
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.717+11539G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611880 | ||||||
chr14:52612082
|
G | C | 3 | a0001c0001t0001g0218a0001c0001t0015g0217a0003c0003t0001g0143 | 3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+11741G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612082 | ||||||
chr14:52612205
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.717+11864G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612205 | ||||||
chr14:52612321
|
A | C | 318 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(315): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.717+11980A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612321 | ||||||
chr14:52612480
|
G | A | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.717+12139G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612480 | ||||||
chr14:52612568
|
T | C | 1 | a0003c0003t0011g0282 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.717+12227T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612568 | ||||||
chr14:52612749
|
A | C | 1 | a0002c0002t0001g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.717+12408A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612749 | ||||||
chr14:52612853
|
A | C | 1 | a0001c0001t0002g0186 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.717+12512A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612853 | ||||||
chr14:52613105
|
G | A | 1 | a0007c0010t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.717+12764G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613105 | ||||||
chr14:52613234
|
G | A | 6 | a0003c0003t0010g0285a0003c0003t0010g0286a0003c0003t0011g0282others(3): Show | 6 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+12893G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613234 | ||||||
chr14:52613246
|
CA | C | 8 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0186others(5): Show | 8 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+12922delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52613246 | |||||
chr14:52613305
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+12964A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613305 | ||||||
chr14:52613546
|
A | G | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.717+13205A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613546 | ||||||
chr14:52613568
|
T | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0015g0217others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+13227T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613568 | ||||||
chr14:52613634
|
A | T | 1 | a0008c0011t0002g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+13293A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613634 | ||||||
chr14:52613873
|
A | G | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.717+13532A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613873 | ||||||
chr14:52614006
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.717+13665C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614006 | ||||||
chr14:52614081
|
G | C | 4 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0015g0217others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+13740G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614081 | ||||||
chr14:52614123
|
C | CT | 12 | a0001c0001t0001g0165a0002c0002t0001g0054a0002c0002t0001g0056others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+13796dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52614123 | |||||
chr14:52614161
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+13820C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614161 | ||||||
chr14:52614198
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.717+13857G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614198 | ||||||
chr14:52614207
|
A | T | 3 | a0001c0001t0001g0218a0001c0001t0015g0217a0003c0003t0001g0143 | 3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+13866A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614207 | ||||||
chr14:52614223
|
C | G | 1 | a0001c0001t0002g0180 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.717+13882C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614223 | ||||||
chr14:52614260
|
G | A | 2 | a0002c0002t0001g0088a0002c0002t0001g0113 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.717+13919G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614260 | ||||||
chr14:52614369
|
C | T | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.717+14028C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614369 | ||||||
chr14:52614487
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0166others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+14146T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614487 | ||||||
chr14:52614561
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.717+14220C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614561 | ||||||
chr14:52614683
|
C | G | 1 | a0001c0001t0003g0320 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.717+14342C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614683 | ||||||
chr14:52614803
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0015g0217a0003c0003t0001g0143 | 3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+14462G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614803 | ||||||
chr14:52614892
|
T | G | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+14551T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614892 | ||||||
chr14:52615087
|
G | A | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.717+14746G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615087 | ||||||
chr14:52615157
|
C | G | 1 | a0004c0004t0001g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.717+14816C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615157 | ||||||
chr14:52615467
|
G | GT | 84 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0014others(81): Show | 88 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.717+15140dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52615467 | |||||
chr14:52615467
|
G | GTT | 105 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0266others(102): Show | 109 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.717+15139_717+1514 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52615467 | |||||
chr14:52615774
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+15433G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615774 | ||||||
chr14:52615833
|
T | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0012others(101): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.717+15492T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615833 | ||||||
chr14:52615995
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0145others(13): Show | 17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.717+15654A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615995 | ||||||
chr14:52616049
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+15708A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616049 | ||||||
chr14:52616283
|
T | TTTTG | 68 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(65): Show | 70 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.718-15853_718-1585 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52616283 | |||||
chr14:52616458
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.718-15702C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616458 | ||||||
chr14:52616472
|
G | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-15688G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616472 | ||||||
chr14:52616495
|
C | T | 329 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(326): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.718-15665C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616495 | ||||||
chr14:52616574
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-15586G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616574 | ||||||
chr14:52616758
|
A | G | 2 | a0002c0002t0001g0287a0002c0002t0001g0288 | 2 | HG01496.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.718-15402A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616758 | ||||||
chr14:52616806
|
A | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(50): Show | 54 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.718-15354A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616806 | ||||||
chr14:52616838
|
G | A | 10 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(7): Show | 14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-15322G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616838 | ||||||
chr14:52616939
|
A | C | 1 | a0002c0002t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.718-15221A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616939 | ||||||
chr14:52617129
|
A | G | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-15031A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617129 | ||||||
chr14:52617208
|
T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-14952T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617208 | ||||||
chr14:52617397
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-14763G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617397 | ||||||
chr14:52617401
|
G | A | 2 | a0001c0001t0002g0194a0008c0011t0002g0174 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.718-14759G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617401 | ||||||
chr14:52617510
|
C | T | 106 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0012others(103): Show | 110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.718-14650C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617510 | ||||||
chr14:52617590
|
C | A | 248 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(245): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.718-14570C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617590 | ||||||
chr14:52617609
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.718-14551G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617609 | ||||||
chr14:52617924
|
G | A | 3 | a0001c0001t0010g0168a0003c0003t0010g0285a0003c0003t0010g0286 | 3 | HG03453.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.718-14236G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617924 | ||||||
chr14:52617946
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.718-14214A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617946 | ||||||
chr14:52617950
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.718-14210C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617950 | ||||||
chr14:52618032
|
G | A | 1 | a0001c0006t0006g0161 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.718-14128G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618032 | ||||||
chr14:52618035
|
G | A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-14125G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | ||||||
chr14:52618035
|
G | C | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-14125G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | ||||||
chr14:52618035
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0280 | 2 | HG02155.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.718-14125G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | ||||||
chr14:52618124
|
A | G | 2 | a0002c0002t0001g0100a0002c0002t0020g0144 | 2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.718-14036A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618124 | ||||||
chr14:52618220
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0145others(13): Show | 17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-13940A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618220 | ||||||
chr14:52618326
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.718-13834A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618326 | ||||||
chr14:52618646
|
G | A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-13514G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618646 | ||||||
chr14:52618681
|
C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-13479C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618681 | ||||||
chr14:52618833
|
G | A | 8 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(5): Show | 10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.718-13327G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618833 | ||||||
chr14:52619022
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.718-13138C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619022 | ||||||
chr14:52619559
|
C | T | 11 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0229others(8): Show | 11 | HG00408.hp1 NA18747.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.718-12601C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619559 | ||||||
chr14:52619725
|
T | A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-12435T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619725 | ||||||
chr14:52620054
|
G | A | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.718-12106G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620054 | ||||||
chr14:52620082
|
G | T | 2 | a0002c0002t0012g0050a0002c0002t0012g0051 | 2 | HG01099.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.718-12078G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620082 | ||||||
chr14:52620195
|
A | G | 107 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0002others(104): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-11965A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620195 | ||||||
chr14:52620262
|
TAGA | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0005c0009t0001g0269 | 3 | NA18960.hp2 NA18964.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.718-11891_718-1188 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52620262 | |||||
chr14:52620483
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.718-11677A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620483 | ||||||
chr14:52620530
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0014others(181): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.718-11630G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620530 | ||||||
chr14:52620946
|
T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-11214T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620946 | ||||||
chr14:52620973
|
A | G | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-11187A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620973 | ||||||
chr14:52621035
|
A | G | 14 | a0001c0001t0002g0189a0001c0001t0002g0190a0002c0002t0001g0069others(11): Show | 14 | HG01167.hp1 HG01496.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-11125A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621035 | ||||||
chr14:52621049
|
T | A | 8 | a0001c0001t0010g0168a0003c0003t0009g0047a0003c0003t0010g0285others(5): Show | 8 | HG02622.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-11111T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621049 | ||||||
chr14:52621351
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.718-10809T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621351 | ||||||
chr14:52621679
|
T | G | 1 | a0001c0001t0001g0238 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.718-10481T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621679 | ||||||
chr14:52621741
|
T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-10419T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621741 | ||||||
chr14:52622602
|
A | T | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-9558A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622602 | ||||||
chr14:52622777
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0145others(13): Show | 17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-9383C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622777 | ||||||
chr14:52622862
|
C | T | 11 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(8): Show | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-9298C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622862 | ||||||
chr14:52622903
|
G | T | 52 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0043others(49): Show | 53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-9257G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622903 | ||||||
chr14:52623036
|
T | C | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-9124T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623036 | ||||||
chr14:52623234
|
C | A | 322 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.718-8926C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623234 | ||||||
chr14:52623273
|
A | T | 1 | a0004c0004t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.718-8887A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623273 | ||||||
chr14:52623277
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0015g0217 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-8883T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623277 | ||||||
chr14:52623667
|
C | CTTCATAA others(6): Show |
320 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(317): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.718-8492_718-8480d others(15): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623667 | |||||
chr14:52623687
|
A | ATTTTCAT others(3): Show |
1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-8469_718-8468i others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623687 | |||||
chr14:52623894
|
TTCATTA | T | 11 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(8): Show | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-8259_718-8254d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623894 | |||||
chr14:52624129
|
C | T | 1 | a0001c0001t0003g0326 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.718-8031C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624129 | ||||||
chr14:52624163
|
G | A | 2 | a0002c0002t0001g0092a0002c0002t0001g0120 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.718-7997G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624163 | ||||||
chr14:52624215
|
T | TA | 79 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(76): Show | 85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.718-7931dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624215 | |||||
chr14:52624399
|
A | C | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.718-7761A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624399 | ||||||
chr14:52624428
|
A | G | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718-7732A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624428 | ||||||
chr14:52624580
|
C | G | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-7580C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624580 | ||||||
chr14:52624580
|
CG | C | 107 | a0001c0006t0006g0163a0002c0002t0001g0001a0002c0002t0001g0002others(104): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-7577delG | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624580 | |||||
chr14:52624581
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.718-7579G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624581 | ||||||
chr14:52624641
|
C | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.718-7519C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624641 | ||||||
chr14:52624700
|
C | T | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718-7460C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624700 | ||||||
chr14:52624711
|
C | T | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-7449C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624711 | ||||||
chr14:52624723
|
C | CA | 122 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0027others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.718-7423dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624723 | |||||
chr14:52624723
|
CA | C | 12 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0049others(9): Show | 14 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-7423delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624723 | |||||
chr14:52624739
|
T | A | 2 | a0001c0001t0001g0218a0003c0003t0001g0143 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-7421T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624739 | ||||||
chr14:52624740
|
G | C | 2 | a0001c0001t0001g0218a0003c0003t0001g0143 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-7420G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624740 | ||||||
chr14:52624823
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-7337C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624823 | ||||||
chr14:52624871
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-7289A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624871 | ||||||
chr14:52625211
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.718-6949C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625211 | ||||||
chr14:52625233
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-6927C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625233 | ||||||
chr14:52625254
|
C | T | 1 | a0004c0004t0001g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.718-6906C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625254 | ||||||
chr14:52625255
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.718-6905G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625255 | ||||||
chr14:52625317
|
A | C | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-6843A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625317 | ||||||
chr14:52625352
|
C | T | 2 | a0004c0004t0001g0198a0004c0004t0001g0274 | 2 | NA18953.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.718-6808C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625352 | ||||||
chr14:52625481
|
C | CA | 7 | a0001c0001t0001g0225a0001c0005t0005g0007a0001c0005t0005g0008others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-6665dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625481 | |||||
chr14:52625532
|
CT | C | 19 | a0001c0006t0006g0160a0002c0002t0001g0002a0002c0002t0001g0054others(16): Show | 21 | HG01071.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.718-6588delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTT | C | 40 | a0001c0001t0001g0241a0002c0002t0001g0046a0002c0002t0001g0056others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.718-6589_718-6588d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTT | C | 23 | a0001c0001t0001g0145a0002c0002t0001g0001a0002c0002t0001g0012others(20): Show | 25 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-6590_718-6588d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTT | C | 11 | a0001c0001t0001g0207a0001c0001t0001g0279a0002c0002t0001g0063others(8): Show | 11 | HG00323.hp1 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.718-6591_718-6588d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTT | C | 12 | a0001c0001t0001g0206a0001c0001t0001g0215a0001c0001t0001g0224others(9): Show | 12 | HG01261.hp1 HG01433.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.718-6592_718-6588d others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTT | C | 37 | a0001c0001t0001g0021a0001c0001t0001g0164a0001c0001t0001g0165others(34): Show | 37 | HG00099.hp2 HG00621.hp1 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.718-6593_718-6588d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0169others(27): Show | 32 | HG00408.hp1 HG00558.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.718-6594_718-6588d others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(1): Show |
C | 37 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0016others(34): Show | 40 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.718-6595_718-6588d others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(10): Show | 13 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.718-6596_718-6588d others(11): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0025g0193a0001c0005t0007g0296 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.718-6597_718-6588d others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0297 | 5 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-6598_718-6588d others(13): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-6599_718-6588d others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0186others(10): Show | 13 | HG00621.hp2 HG01978.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.718-6602_718-6588d others(17): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(9): Show |
C | 59 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0024others(56): Show | 61 | HG00280.hp1 HG00438.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.718-6603_718-6588d others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.718-6604_718-6588d others(19): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.718-6605_718-6588d others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(15): Show |
C | 3 | a0002c0002t0001g0099a0002c0002t0001g0128a0002c0002t0001g0129 | 3 | NA18957.hp1 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.718-6609_718-6588d others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625532
|
CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0001g0045a0001c0001t0015g0217 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-6612_718-6588d others(27): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | |||||
chr14:52625573
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-6587G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625573 | ||||||
chr14:52625577
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.718-6583C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625577 | ||||||
chr14:52625703
|
C | T | 1 | a0002c0002t0012g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.718-6457C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625703 | ||||||
chr14:52625715
|
C | T | 1 | a0001c0005t0005g0202 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.718-6445C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625715 | ||||||
chr14:52625776
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-6384G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625776 | ||||||
chr14:52625806
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0221others(5): Show | 9 | HG00558.hp1 HG02015.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-6354G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625806 | ||||||
chr14:52625850
|
G | T | 6 | a0001c0001t0010g0168a0003c0003t0010g0285a0003c0003t0010g0286others(3): Show | 6 | HG02717.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-6310G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625850 | ||||||
chr14:52625950
|
C | G | 1 | a0001c0001t0016g0192 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-6210C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625950 | ||||||
chr14:52625977
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-6183A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625977 | ||||||
chr14:52625998
|
A | G | 1 | a0003c0003t0002g0094 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.718-6162A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625998 | ||||||
chr14:52626002
|
A | G | 10 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(7): Show | 14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-6158A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626002 | ||||||
chr14:52626007
|
C | T | 11 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(8): Show | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-6153C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626007 | ||||||
chr14:52626455
|
T | TA | 16 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0294others(13): Show | 20 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.718-5693dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52626455 | |||||
chr14:52626479
|
A | G | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0277 | 3 | HG02071.hp2 NA18962.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.718-5681A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626479 | ||||||
chr14:52626794
|
A | C | 12 | a0001c0001t0025g0193a0001c0005t0005g0007a0001c0005t0005g0008others(9): Show | 16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-5366A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626794 | ||||||
chr14:52626912
|
A | G | 3 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0155 | 3 | HG02976.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-5248A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626912 | ||||||
chr14:52626934
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.718-5226C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626934 | ||||||
chr14:52627060
|
A | G | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-5100A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627060 | ||||||
chr14:52627096
|
T | A | 1 | a0001c0001t0001g0252 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.718-5064T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627096 | ||||||
chr14:52627292
|
C | G | 144 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(141): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.718-4868C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627292 | ||||||
chr14:52627324
|
T | A | 1 | a0001c0001t0002g0194 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.718-4836T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627324 | ||||||
chr14:52627391
|
T | C | 1 | a0001c0001t0015g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.718-4769T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627391 | ||||||
chr14:52627507
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0164others(12): Show | 16 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.718-4653G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627507 | ||||||
chr14:52627526
|
C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.718-4634C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627526 | ||||||
chr14:52627569
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.718-4591C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627569 | ||||||
chr14:52627575
|
G | A | 1 | a0001c0001t0003g0301 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.718-4585G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627575 | ||||||
chr14:52627592
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.718-4568A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627592 | ||||||
chr14:52627759
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-4401G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627759 | ||||||
chr14:52627837
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.718-4323C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627837 | ||||||
chr14:52627877
|
G | A | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.718-4283G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627877 | ||||||
chr14:52627903
|
T | C | 3 | a0003c0003t0011g0282a0003c0003t0011g0283a0003c0003t0011g0284 | 3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.718-4257T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627903 | ||||||
chr14:52628003
|
A | G | 2 | a0001c0001t0013g0167a0001c0001t0013g0172 | 2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.718-4157A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628003 | ||||||
chr14:52628104
|
T | C | 73 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0024others(70): Show | 75 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.718-4056T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628104 | ||||||
chr14:52628127
|
A | G | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.718-4033A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628127 | ||||||
chr14:52628139
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-4021G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628139 | ||||||
chr14:52628141
|
G | A | 7 | a0002c0002t0001g0012a0002c0002t0001g0062a0002c0002t0001g0063others(4): Show | 7 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-4019G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628141 | ||||||
chr14:52628303
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.718-3857T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628303 | ||||||
chr14:52628472
|
G | C | 1 | a0002c0002t0001g0129 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.718-3688G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628472 | ||||||
chr14:52628489
|
A | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0016g0192 | 3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-3671A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628489 | ||||||
chr14:52628546
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.718-3614A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628546 | ||||||
chr14:52628884
|
C | T | 6 | a0002c0002t0001g0052a0002c0002t0001g0119a0002c0002t0001g0121others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-3276C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628884 | ||||||
chr14:52628887
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.718-3273A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628887 | ||||||
chr14:52628899
|
A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-3261A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628899 | ||||||
chr14:52628977
|
G | T | 1 | a0001c0001t0003g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.718-3183G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628977 | ||||||
chr14:52628988
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.718-3172A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628988 | ||||||
chr14:52629009
|
C | T | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-3151C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629009 | ||||||
chr14:52629367
|
C | T | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-2793C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629367 | ||||||
chr14:52629580
|
A | G | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2580A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629580 | ||||||
chr14:52629603
|
A | G | 12 | a0001c0001t0025g0193a0001c0005t0005g0007a0001c0005t0005g0008others(9): Show | 16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-2557A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629603 | ||||||
chr14:52629632
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.718-2528A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629632 | ||||||
chr14:52629703
|
T | C | 1 | a0001c0001t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.718-2457T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629703 | ||||||
chr14:52629817
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0166others(8): Show | 12 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.718-2343C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629817 | ||||||
chr14:52629853
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0015g0217 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-2307A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629853 | ||||||
chr14:52629887
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-2273G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629887 | ||||||
chr14:52629939
|
G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-2221G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629939 | ||||||
chr14:52629950
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.718-2210C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629950 | ||||||
chr14:52630054
|
C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-2106C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630054 | ||||||
chr14:52630125
|
G | A | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-2035G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630125 | ||||||
chr14:52630189
|
C | T | 1 | a0001c0005t0005g0203 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.718-1971C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630189 | ||||||
chr14:52630200
|
C | A | 11 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(8): Show | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1960C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630200 | ||||||
chr14:52630446
|
C | CTT | 11 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(8): Show | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1711_718-1710d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630446 | |||||
chr14:52630453
|
T | TAAC | 28 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0145others(25): Show | 33 | HG00738.hp2 HG01074.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.718-1706_718-1704d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630453 | |||||
chr14:52630491
|
G | T | 107 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0002others(104): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-1669G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630491 | ||||||
chr14:52630694
|
ACCCCGCA others(4): Show |
A | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-1455_718-1445d others(13): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630694 | |||||
chr14:52630709
|
C | T | 7 | a0002c0002t0001g0069a0002c0002t0001g0099a0004c0004t0001g0013others(4): Show | 7 | HG01496.hp1 HG01993.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-1451C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630709 | ||||||
chr14:52630888
|
A | G | 2 | a0001c0001t0001g0218a0003c0003t0001g0143 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-1272A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630888 | ||||||
chr14:52630994
|
G | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0012others(101): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.718-1166G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630994 | ||||||
chr14:52631090
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1070A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631090 | ||||||
chr14:52631091
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0169a0003c0003t0001g0103others(1): Show | 5 | HG01074.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1069T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631091 | ||||||
chr14:52631142
|
G | A | 9 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(6): Show | 9 | HG02080.hp2 NA18747.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-1018G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631142 | ||||||
chr14:52631305
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-855C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631305 | ||||||
chr14:52631339
|
C | G | 1 | a0001c0001t0009g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-821C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631339 | ||||||
chr14:52631394
|
A | G | 1 | a0001c0001t0009g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-766A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631394 | ||||||
chr14:52631438
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0016g0192 | 3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-722C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631438 | ||||||
chr14:52631828
|
G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0195 | 2 | NA20129.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.718-332G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631828 | ||||||
chr14:52631854
|
C | T | 2 | a0001c0001t0003g0326a0001c0001t0003g0329 | 2 | NA18991.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.718-306C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631854 | ||||||
chr14:52631953
|
CA | C | 148 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(145): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.718-191delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52631953 | |||||
chr14:52631953
|
CAA | C | 8 | a0001c0001t0010g0168a0002c0002t0001g0062a0002c0002t0001g0064others(5): Show | 8 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-192_718-191del others(2): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52631953 | |||||
chr14:52632069
|
A | C | 1 | a0001c0001t0025g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-91A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52632069 | ||||||
chr14:52632111
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0016g0192 | 3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-49C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52632111 | ||||||
chr14:52632350
|
ATTAAC | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0233a0001c0001t0001g0237 | 3 | NA18971.hp2 NA19005.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.867+45_867+49delAC others(3): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 52632350 | |||||
chr14:52632390
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0008g0310 | 3 | HG00438.hp2 NA18947.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.867+81C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632390 | ||||||
chr14:52632532
|
T | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.867+223T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632532 | ||||||
chr14:52632541
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.867+232T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632541 | ||||||
chr14:52632575
|
T | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0145others(13): Show | 17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+266T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632575 | ||||||
chr14:52632577
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.867+268A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632577 | ||||||
chr14:52632760
|
G | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.867+451G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632760 | ||||||
chr14:52632821
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0019g0038 | 2 | NA18980.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.867+512A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632821 | ||||||
chr14:52632946
|
T | A | 4 | a0001c0005t0007g0003a0001c0005t0007g0295a0001c0005t0007g0296others(1): Show | 6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-584T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632946 | ||||||
chr14:52632955
|
C | T | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-575C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632955 | ||||||
chr14:52633116
|
G | A | 1 | a0001c0001t0013g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.868-414G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52633116 | ||||||
chr14:52633234
|
T | C | 6 | a0001c0005t0005g0007a0001c0005t0005g0008a0001c0005t0005g0200others(3): Show | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-296T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52633234 | ||||||
chr14:52634042
|
A | G | 172 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1112+96A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634042 | ||||||
chr14:52634106
|
A | G | 2 | a0001c0001t0001g0218a0003c0003t0001g0143 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1112+160A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634106 | ||||||
chr14:52634152
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1112+206A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634152 | ||||||
chr14:52634212
|
G | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0040others(7): Show | 10 | HG00423.hp2 HG00609.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1112+266G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634212 | ||||||
chr14:52634531
|
C | A | 1 | a0001c0001t0002g0194 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113-407C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634531 | ||||||
chr14:52634834
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1113-104T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634834 | ||||||
chr14:52634863
|
A | G | 3 | a0002c0002t0012g0050a0002c0002t0012g0051a0002c0002t0012g0109 | 3 | HG01099.hp2 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1113-75A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634863 | ||||||
chr14:52634904
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1113-34G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634904 |