geneid | 54542 |
---|---|
ensemblid | ENSG00000056586.16 |
hgncid | 21461 |
symbol | RC3H2 |
name | ring finger and CCCH-type domains 2 |
refseq_nuc | NM_001100588.3 |
refseq_prot | NP_001094058.1 |
ensembl_nuc | ENST00000357244.7 |
ensembl_prot | ENSP00000349783.2 |
mane_status | MANE Select |
chr | chr9 |
start | 122844556 |
end | 122905359 |
strand | - |
ver | v1.2 |
region | chr9:122844556-122905359 |
region5000 | chr9:122839556-122910359 |
regionname0 | RC3H2_chr9_122844556_122905359 |
regionname5000 | RC3H2_chr9_122839556_122910359 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1191 | 308 | 83 | 66 | 108 | 16 | 33 | 77 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0002 | 0/0 | 1191 | 10 | 1 | 0 | 9 | 0 | 0 | 7 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0003 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0004 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3576 | 186 | 49 | 39 | 52 | 14 | 30 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0002 | 0/0 | 3576 | 101 | 22 | 21 | 54 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0003 | 0/0 | 3576 | 10 | 1 | 0 | 9 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0004 | 0/0 | 3576 | 8 | 7 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0005 | 0/0 | 3576 | 7 | 3 | 3 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0006 | 0/0 | 3576 | 2 | 1 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0007 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0008 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0009 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0010 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0011 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
c0012 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5391 | 128 | 29 | 28 | 36 | 12 | 22 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0002 | 0/0 | 5391 | 103 | 21 | 21 | 57 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0003 | 0/0 | 5391 | 21 | 1 | 9 | 5 | 1 | 5 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0004 | 0/0 | 5391 | 15 | 10 | 4 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0005 | 0/0 | 5391 | 9 | 9 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0006 | 0/0 | 5391 | 6 | 0 | 0 | 6 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0007 | 0/0 | 5391 | 5 | 0 | 0 | 5 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0008 | 0/0 | 5391 | 3 | 0 | 0 | 3 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0009 | 0/0 | 5392 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0010 | 0/0 | 5391 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0011 | 0/0 | 5391 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0012 | 0/0 | 5392 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0013 | 0/0 | 5391 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0014 | 0/0 | 5391 | 2 | 0 | 0 | 0 | 0 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0015 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0016 | 0/0 | 5392 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0017 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0018 | 0/0 | 5391 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0019 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0020 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0021 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0022 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0023 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0024 | 0/0 | 5391 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0025 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0026 | 0/0 | 5391 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0027 | 1/0 | 5389 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0028 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
t0029 | 0/0 | 5391 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3576 | 186 | 49 | 39 | 52 | 14 | 30 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002 | 0/0 | 3576 | 101 | 22 | 21 | 54 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0004 | 0/0 | 3576 | 8 | 7 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0005 | 0/0 | 3576 | 7 | 3 | 3 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0006 | 0/0 | 3576 | 2 | 1 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0007 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0010 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0011 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0012 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0002c0003 | 0/0 | 3576 | 10 | 1 | 0 | 9 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0003c0008 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0004c0009 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8966 | 125 | 29 | 28 | 34 | 12 | 21 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0003 | 0/0 | 8966 | 21 | 1 | 9 | 5 | 1 | 5 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0005 | 0/0 | 8966 | 8 | 8 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0006 | 0/0 | 8966 | 6 | 0 | 0 | 6 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0007 | 0/0 | 8966 | 5 | 0 | 0 | 5 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0009 | 0/0 | 8967 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0010 | 0/0 | 8966 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0011 | 0/0 | 8966 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0013 | 0/0 | 8966 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0014 | 0/0 | 8966 | 2 | 0 | 0 | 0 | 0 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0017 | 0/0 | 8966 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0019 | 0/0 | 8966 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0023 | 0/0 | 8966 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0025 | 0/0 | 8966 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0026 | 0/0 | 8966 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0027 | 1/0 | 8964 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0028 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0001t0029 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0002 | 0/0 | 8966 | 93 | 21 | 20 | 48 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0008 | 0/0 | 8966 | 3 | 0 | 0 | 3 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0012 | 0/0 | 8967 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0016 | 0/0 | 8967 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0018 | 0/0 | 8966 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0022 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0002t0024 | 0/0 | 8966 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0004t0004 | 0/0 | 8966 | 8 | 7 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0005t0004 | 0/0 | 8966 | 7 | 3 | 3 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0006t0015 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0006t0021 | 0/0 | 8966 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0007t0005 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0010t0001 | 0/0 | 8966 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0011t0002 | 0/0 | 8966 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0001c0012t0002 | 0/0 | 8966 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0002c0003t0002 | 0/0 | 8966 | 8 | 0 | 0 | 8 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0002c0003t0012 | 0/0 | 8967 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0002c0003t0020 | 0/0 | 8966 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0003c0008t0001 | 0/0 | 8966 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
a0004c0009t0001 | 0/0 | 8966 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | copy fasta | chr9 | 122839556 | 122910359 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0009g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0014g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0014g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0017g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0019g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0025g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0026g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0027g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0028g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0001t0029g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0018g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0002t0024g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0004t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0005t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0006t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0006t0021g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0007t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0010t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0011t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0001c0012t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0012g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0002c0003t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0003c0008t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
a0004c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00140 | hp1 | a0001 | c0001 | t0023 | g0251 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00323 | hp2 | a0001 | c0005 | t0004 | g0047 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00544 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00639 | hp2 | a0001 | c0006 | t0021 | g0299 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00738 | hp2 | a0001 | c0005 | t0004 | g0118 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0291 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01099 | hp1 | a0001 | c0001 | t0019 | g0257 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01099 | hp2 | a0001 | c0005 | t0004 | g0121 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01109 | hp2 | a0001 | c0011 | t0002 | g0109 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01175 | hp2 | a0001 | c0005 | t0004 | g0046 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01243 | hp1 | a0001 | c0002 | t0024 | g0055 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0292 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01433 | hp1 | a0001 | c0001 | t0017 | g0214 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01496 | hp1 | a0001 | c0004 | t0004 | g0089 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01891 | hp1 | a0001 | c0001 | t0029 | g0152 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0198 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0137 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02155 | hp1 | a0002 | c0003 | t0002 | g0016 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02165 | hp2 | a0001 | c0012 | t0002 | g0093 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02257 | hp2 | a0001 | c0005 | t0004 | g0052 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02258 | hp1 | a0001 | c0004 | t0004 | g0115 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0091 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02451 | hp1 | a0001 | c0004 | t0004 | g0012 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0300 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02523 | hp2 | a0004 | c0009 | t0001 | g0289 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02602 | hp2 | a0001 | c0001 | t0026 | g0221 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0196 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0197 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02723 | hp1 | a0001 | c0006 | t0015 | g0010 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0078 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02818 | hp2 | a0001 | c0005 | t0004 | g0090 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02895 | hp1 | a0001 | c0005 | t0004 | g0120 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0237 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03139 | hp1 | a0002 | c0003 | t0020 | g0022 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03209 | hp1 | a0001 | c0002 | t0022 | g0124 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03239 | hp1 | a0001 | c0001 | t0014 | g0304 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03486 | hp2 | a0001 | c0004 | t0004 | g0297 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03491 | hp1 | a0001 | c0001 | t0025 | g0264 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03540 | hp1 | a0001 | c0004 | t0004 | g0122 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0151 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0079 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04199 | hp1 | a0003 | c0008 | t0001 | g0035 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0253 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04204 | hp1 | a0001 | c0001 | t0014 | g0303 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | CHB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18945 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0307 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18947 | hp1 | a0001 | c0002 | t0012 | g0106 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18947 | hp2 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18956 | hp2 | a0001 | c0002 | t0008 | g0062 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18957 | hp1 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0021 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18963 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18964 | hp2 | a0001 | c0002 | t0018 | g0086 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18971 | hp1 | a0002 | c0003 | t0002 | g0017 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18978 | hp2 | a0001 | c0010 | t0001 | g0218 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18986 | hp1 | a0001 | c0002 | t0008 | g0064 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18992 | hp1 | a0001 | c0001 | t0013 | g0155 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19001 | hp2 | a0001 | c0001 | t0007 | g0309 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19004 | hp2 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19011 | hp2 | a0001 | c0001 | t0013 | g0153 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19043 | hp1 | a0001 | c0001 | t0028 | g0294 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19043 | hp2 | a0001 | c0004 | t0004 | g0119 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19068 | hp1 | a0001 | c0002 | t0016 | g0063 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19068 | hp2 | a0002 | c0003 | t0012 | g0019 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0274 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0306 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | ASW | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | ASW | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0104 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | GIH | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02109 | hp2 | a0001 | c0004 | t0004 | g0117 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02559 | hp1 | a0001 | c0004 | t0004 | g0116 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
HG06807 | hp2 | a0001 | c0007 | t0005 | g0045 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0305 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0041 | REF | REF | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0027 | g0169 | REF | REF | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122854242
|
T | G | 1 | a0003 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2925A>C | p.Leu975Phe | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/21 | 3242/8964 | 2925/3576 | 975/1191 | chr9 | 122854242 | ||
chr9:122858958
|
T | C | 1 | a0004 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1994A>G | p.Asp665Gly | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/21 | 2311/8964 | 1994/3576 | 665/1191 | chr9 | 122858958 | ||
chr9:122897437
|
C | T | 1 | a0002 | 10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.73G>A | p.Val25Met | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/21 | 390/8964 | 73/3576 | 25/1191 | chr9 | 122897437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122854602
|
A | G | 1 | a0001c0007 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2829T>C | p.Tyr943Tyr | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 16/21 | 3146/8964 | 2829/3576 | 943/1191 | chr9 | 122854602 | ||
chr9:122855801
|
T | G | 2 | a0001c0004a0001c0005 | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
synonymous_variant | LOW | c.2532A>C | p.Ile844Ile | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 14/21 | 2849/8964 | 2532/3576 | 844/1191 | chr9 | 122855801 | ||
chr9:122857932
|
A | G | 1 | a0001c0004 | 8 | HG01496.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
synonymous_variant | LOW | c.2445T>C | p.Phe815Phe | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/21 | 2762/8964 | 2445/3576 | 815/1191 | chr9 | 122857932 | ||
chr9:122859068
|
A | G | 1 | a0001c0006 | 2 | HG00639.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.1884T>C | p.Gly628Gly | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/21 | 2201/8964 | 1884/3576 | 628/1191 | chr9 | 122859068 | ||
chr9:122880069
|
T | C | 1 | a0001c0012 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1017A>G | p.Gln339Gln | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 7/21 | 1334/8964 | 1017/3576 | 339/1191 | chr9 | 122880069 | ||
chr9:122880603
|
G | A | 1 | a0001c0010 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.951C>T | p.Ile317Ile | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/21 | 1268/8964 | 951/3576 | 317/1191 | chr9 | 122880603 | ||
chr9:122890393
|
A | G | 1 | a0001c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.502T>C | p.Leu168Leu | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/21 | 819/8964 | 502/3576 | 168/1191 | chr9 | 122890393 | ||
chr9:122890478
|
G | A | 6 | a0001c0002a0001c0004a0001c0005others(3): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
synonymous_variant | LOW | c.417C>T | p.Asn139Asn | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/21 | 734/8964 | 417/3576 | 139/1191 | chr9 | 122890478 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122844683
|
A | G | 2 | a0001c0006t0015a0001c0006t0021 | 2 | HG00639.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4944T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4944 | chr9 | 122844683 | |||||
chr9:122844732
|
T | C | 14 | a0001c0002t0002a0001c0002t0008a0001c0002t0012others(11): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*4895A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4895 | chr9 | 122844732 | |||||
chr9:122844882
|
G | C | 1 | a0001c0001t0014 | 2 | HG03239.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4745C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4745 | chr9 | 122844882 | |||||
chr9:122845486
|
T | C | 1 | a0001c0002t0022 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4141A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4141 | chr9 | 122845486 | |||||
chr9:122845524
|
T | C | 1 | a0001c0001t0023 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4103A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4103 | chr9 | 122845524 | |||||
chr9:122845954
|
T | C | 1 | a0001c0002t0024 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3673A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3673 | chr9 | 122845954 | |||||
chr9:122845972
|
A | G | 1 | a0002c0003t0020 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3655T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3655 | chr9 | 122845972 | |||||
chr9:122846073
|
A | G | 2 | a0001c0001t0005a0001c0007t0005 | 9 | HG02145.hp2 HG02809.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3554T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3554 | chr9 | 122846073 | |||||
chr9:122846343
|
T | C | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3284A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3284 | chr9 | 122846343 | |||||
chr9:122846348
|
T | C | 1 | a0001c0001t0003 | 21 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3279A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3279 | chr9 | 122846348 | |||||
chr9:122846464
|
A | T | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3163T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3163 | chr9 | 122846464 | |||||
chr9:122846707
|
T | C | 2 | a0001c0001t0019a0001c0001t0025 | 2 | HG01099.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2920A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2920 | chr9 | 122846707 | |||||
chr9:122846786
|
C | G | 1 | a0001c0001t0010 | 3 | HG02622.hp2 HG02630.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2841G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2841 | chr9 | 122846786 | |||||
chr9:122847067
|
G | T | 1 | a0001c0001t0019 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2560 | chr9 | 122847067 | |||||
chr9:122847078
|
G | A | 1 | a0001c0001t0026 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2549 | chr9 | 122847078 | |||||
chr9:122847263
|
A | G | 1 | a0001c0002t0018 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2364 | chr9 | 122847263 | |||||
chr9:122847282
|
C | T | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2345 | chr9 | 122847282 | |||||
chr9:122847653
|
A | AAT | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(34): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1973_*1974insAT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1973 | chr9 | 122847653 | |||||
chr9:122847772
|
C | G | 1 | a0001c0001t0006 | 6 | HG00408.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1855G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1855 | chr9 | 122847772 | |||||
chr9:122848134
|
G | A | 1 | a0001c0001t0029 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1493 | chr9 | 122848134 | |||||
chr9:122848455
|
T | C | 1 | a0001c0001t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1172 | chr9 | 122848455 | |||||
chr9:122848696
|
G | A | 2 | a0001c0004t0004a0001c0005t0004 | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*931C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 931 | chr9 | 122848696 | |||||
chr9:122849090
|
T | C | 2 | a0001c0001t0011a0001c0001t0029 | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 537 | chr9 | 122849090 | |||||
chr9:122849441
|
C | CT | 4 | a0001c0001t0009a0001c0002t0012a0001c0002t0016others(1): Show | 6 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*185dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 185 | chr9 | 122849441 | |||||
chr9:122849453
|
C | T | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 174 | chr9 | 122849453 | |||||
chr9:122897557
|
G | T | 2 | a0001c0002t0008a0001c0002t0016 | 4 | NA18956.hp2 NA18957.hp1 NA18986.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-48C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/21 | 48 | chr9 | 122897557 | |||||
chr9:122905148
|
G | A | 1 | a0001c0001t0014 | 2 | HG03239.hp1 HG04204.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | chr9 | 122905148 | ||||||
chr9:122905308
|
C | G | 1 | a0001c0006t0015 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | 7799 | chr9 | 122905308 | |||||
chr9:122905327
|
T | C | 1 | a0001c0001t0007 | 5 | NA18945.hp2 NA18955.hp2 NA18986.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-285A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | 7818 | chr9 | 122905327 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:122849850
|
CAA | C | 75 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(72): Show | 76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.3381-30_3381-29del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122849850 | ||||||
chr9:122850013
|
G | A | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3381-191C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850013 | ||||||
chr9:122850190
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3381-368C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850190 | ||||||
chr9:122850435
|
T | TATAGATA others(5): Show |
12 | a0001c0002t0002g0072a0001c0002t0002g0078a0001c0002t0002g0079others(9): Show | 12 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.3381-625_3381-614d others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | ||||||
chr9:122850435
|
T | TATAGATA others(9): Show |
49 | a0001c0001t0005g0006a0001c0001t0005g0166a0001c0001t0005g0167others(46): Show | 50 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.3381-629_3381-614d others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | ||||||
chr9:122850435
|
T | TATAGATA others(13): Show |
61 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0001g0160others(58): Show | 62 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.3380+626_3381-614d others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | ||||||
chr9:122850435
|
T | TATAGATA others(17): Show |
37 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0158others(34): Show | 38 | HG00544.hp1 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.3381-614_3381-613i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | ||||||
chr9:122850435
|
T | TATAGATA others(21): Show |
1 | a0001c0002t0002g0125 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3381-614_3381-613i others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | ||||||
chr9:122850528
|
C | T | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.3380+553G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850528 | ||||||
chr9:122850625
|
G | A | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3380+456C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850625 | ||||||
chr9:122850628
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0245 | 2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.3380+453C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850628 | ||||||
chr9:122850891
|
T | C | 1 | a0001c0005t0004g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3380+190A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850891 | ||||||
chr9:122851266
|
T | G | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.3232-37A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 19/20 | chr9 | 122851266 | ||||||
chr9:122851611
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0275a0001c0001t0001g0277others(1): Show | 5 | HG00621.hp2 NA18747.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.3118-175G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851611 | ||||||
chr9:122851634
|
T | C | 2 | a0001c0004t0004g0012a0001c0004t0004g0116 | 2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3118-198A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851634 | ||||||
chr9:122851653
|
C | T | 2 | a0001c0001t0009g0237a0001c0001t0009g0239 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3118-217G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851653 | ||||||
chr9:122851669
|
G | C | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3118-233C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851669 | ||||||
chr9:122851687
|
CGGGGTTT others(6): Show |
C | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.3118-264_3118-252d others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851687 | ||||||
chr9:122851688
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3118-252C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851688 | ||||||
chr9:122851859
|
C | A | 1 | a0001c0001t0003g0252 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3118-423G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851859 | ||||||
chr9:122851910
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0023g0251 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.3118-474C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851910 | ||||||
chr9:122851914
|
G | A | 1 | a0001c0006t0021g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3118-478C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851914 | ||||||
chr9:122851936
|
G | C | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118-500C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851936 | ||||||
chr9:122852114
|
G | A | 139 | a0001c0001t0005g0006a0001c0001t0005g0011a0001c0001t0005g0165others(136): Show | 141 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.3118-678C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852114 | ||||||
chr9:122852185
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.3118-749G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852185 | ||||||
chr9:122852189
|
A | AC | 37 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0183others(34): Show | 37 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.3118-754dupG | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852189 | ||||||
chr9:122852250
|
CCTCCGCC others(33): Show |
C | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-854_3118-815d others(42): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852250 | ||||||
chr9:122852275
|
G | C | 1 | a0001c0001t0001g0226 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3118-839C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852275 | ||||||
chr9:122852324
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0223 | 2 | HG01258.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3118-888C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852324 | ||||||
chr9:122852338
|
T | C | 160 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(157): Show | 163 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3118-902A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852338 | ||||||
chr9:122852350
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(277): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.3118-914G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852350 | ||||||
chr9:122852380
|
GCAGCCGC others(42): Show |
G | 1 | a0001c0001t0010g0197 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3118-993_3118-945d others(51): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852380 | ||||||
chr9:122852380
|
GCAGCCGC others(120): Show |
G | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-1071_3118-945 others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852380 | ||||||
chr9:122852386
|
G | A | 4 | a0001c0002t0002g0061a0001c0002t0002g0107a0001c0002t0002g0123others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118-950C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852386 | ||||||
chr9:122852408
|
G | A | 12 | a0001c0001t0005g0006a0001c0001t0005g0011a0001c0001t0005g0165others(9): Show | 13 | HG01891.hp1 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.3118-972C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852408 | ||||||
chr9:122852457
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3118-1021G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852457 | ||||||
chr9:122852521
|
C | T | 20 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(17): Show | 20 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.3118-1085G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852521 | ||||||
chr9:122852549
|
C | CGCCCGGC others(42): Show |
2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3118-1162_3118-111 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852549 | ||||||
chr9:122852619
|
C | T | 2 | a0001c0002t0002g0061a0001c0002t0022g0124 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3118-1183G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852619 | ||||||
chr9:122852682
|
C | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-1246G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852682 | ||||||
chr9:122852729
|
C | A | 3 | a0001c0005t0004g0090a0001c0005t0004g0120a0001c0005t0004g0121 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3117+1223G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852729 | ||||||
chr9:122852746
|
C | T | 4 | a0001c0002t0002g0048a0001c0002t0002g0056a0001c0002t0002g0057others(1): Show | 4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3117+1206G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852746 | ||||||
chr9:122852810
|
G | A | 1 | a0001c0005t0004g0090 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3117+1142C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852810 | ||||||
chr9:122852857
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3117+1095T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852857 | ||||||
chr9:122852941
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3117+1011C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852941 | ||||||
chr9:122852945
|
G | C | 1 | a0001c0001t0003g0206 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3117+1007C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852945 | ||||||
chr9:122852979
|
A | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0147others(25): Show | 29 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.3117+973T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852979 | ||||||
chr9:122853007
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3117+945T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853007 | ||||||
chr9:122853105
|
C | A | 1 | a0001c0002t0008g0049 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3117+847G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853105 | ||||||
chr9:122853125
|
A | G | 13 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3117+827T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853125 | ||||||
chr9:122853135
|
C | A | 13 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3117+817G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853135 | ||||||
chr9:122853191
|
A | C | 16 | a0001c0001t0001g0226a0001c0004t0004g0012a0001c0004t0004g0089others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.3117+761T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853191 | ||||||
chr9:122853191
|
A | G | 12 | a0001c0001t0001g0147a0001c0001t0005g0006a0001c0001t0005g0011others(9): Show | 13 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3117+761T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853191 | ||||||
chr9:122853286
|
T | C | 3 | a0001c0001t0017g0214a0001c0002t0002g0107a0001c0002t0002g0123 | 3 | HG01243.hp2 HG01433.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3117+666A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853286 | ||||||
chr9:122853295
|
T | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0194 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3117+657A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853295 | ||||||
chr9:122853378
|
T | TAA | 70 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.3117+572_3117+573d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | ||||||
chr9:122853378
|
T | TAAA | 55 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(52): Show | 56 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.3117+571_3117+573d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | ||||||
chr9:122853378
|
TA | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0238a0001c0001t0003g0290others(3): Show | 6 | HG01256.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3117+573delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | ||||||
chr9:122853394
|
A | AG | 27 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(24): Show | 29 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.3117+557_3117+558i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853394 | ||||||
chr9:122853394
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3117+558T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853394 | ||||||
chr9:122853398
|
G | A | 7 | a0001c0001t0001g0042a0001c0002t0002g0048a0001c0002t0002g0054others(4): Show | 7 | HG00642.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.3117+554C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853398 | ||||||
chr9:122853414
|
A | G | 1 | a0001c0002t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3117+538T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853414 | ||||||
chr9:122853427
|
C | T | 6 | a0001c0001t0006g0029a0001c0001t0006g0227a0001c0001t0006g0268others(3): Show | 6 | HG00408.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.3117+525G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853427 | ||||||
chr9:122853480
|
G | A | 1 | a0001c0001t0026g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3117+472C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853480 | ||||||
chr9:122853523
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3117+429C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853523 | ||||||
chr9:122853640
|
T | C | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3117+312A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853640 | ||||||
chr9:122854099
|
G | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0023g0251 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2983-13C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854099 | ||||||
chr9:122854102
|
A | G | 1 | a0001c0001t0011g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2983-16T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854102 | ||||||
chr9:122854126
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0023g0251 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2983-40A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854126 | ||||||
chr9:122854411
|
T | G | 1 | a0001c0002t0002g0070 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2900+120A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 16/20 | chr9 | 122854411 | ||||||
chr9:122854758
|
G | A | 123 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(120): Show | 124 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2816-143C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854758 | ||||||
chr9:122854891
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-276C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854891 | ||||||
chr9:122854911
|
C | T | 13 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069others(10): Show | 13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.2815+273G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854911 | ||||||
chr9:122854949
|
T | C | 5 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(2): Show | 5 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2815+235A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854949 | ||||||
chr9:122854973
|
G | A | 126 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(123): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+211C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854973 | ||||||
chr9:122855018
|
G | T | 126 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(123): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+166C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855018 | ||||||
chr9:122855022
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2815+162C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855022 | ||||||
chr9:122855112
|
C | G | 126 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(123): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+72G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855112 | ||||||
chr9:122855116
|
T | TA | 8 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0001g0225others(5): Show | 8 | HG01346.hp2 HG02300.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2815+67dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855116 | ||||||
chr9:122855116
|
TA | T | 140 | a0001c0001t0001g0201a0001c0001t0001g0236a0001c0001t0001g0284others(137): Show | 142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2815+67delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855116 | ||||||
chr9:122855135
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2815+49C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855135 | ||||||
chr9:122855890
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2455-12T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122855890 | ||||||
chr9:122856019
|
T | A | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2455-141A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856019 | ||||||
chr9:122856277
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2455-399C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856277 | ||||||
chr9:122856540
|
C | A | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-662G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856540 | ||||||
chr9:122856556
|
A | G | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2455-678T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856556 | ||||||
chr9:122856629
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0236others(1): Show | 5 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-751C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856629 | ||||||
chr9:122856813
|
C | CA | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-936_2455-935i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856813 | ||||||
chr9:122856814
|
G | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-936C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856814 | ||||||
chr9:122857137
|
C | T | 2 | a0001c0001t0013g0153a0001c0001t0013g0155 | 2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2454+786G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857137 | ||||||
chr9:122857182
|
T | C | 3 | a0001c0001t0003g0205a0001c0001t0003g0246a0001c0001t0003g0247 | 3 | HG02056.hp2 NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2454+741A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857182 | ||||||
chr9:122857459
|
C | A | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454+464G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857459 | ||||||
chr9:122857590
|
A | G | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+333T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857590 | ||||||
chr9:122857826
|
C | CA | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2454+96dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857826 | ||||||
chr9:122858186
|
T | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0023g0251 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2284-93A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/20 | chr9 | 122858186 | ||||||
chr9:122858573
|
C | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2283+96G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/20 | chr9 | 122858573 | ||||||
chr9:122859181
|
C | A | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850-79G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859181 | ||||||
chr9:122859234
|
T | C | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG00099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850-132A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859234 | ||||||
chr9:122859252
|
C | CTTTTTTT | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1850-157_1850-151d others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0160others(11): Show | 14 | HG00323.hp1 HG00738.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1850-158_1850-151d others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0010g0196a0001c0001t0010g0232a0001c0002t0002g0069others(13): Show | 16 | HG01099.hp2 HG01175.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1850-159_1850-151d others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0010g0197a0001c0002t0002g0048a0001c0002t0002g0056others(5): Show | 8 | HG00544.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-160_1850-151d others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(4): Show |
57 | a0001c0001t0001g0147a0001c0002t0002g0004a0001c0002t0002g0051others(54): Show | 58 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1850-161_1850-151d others(13): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(5): Show |
26 | a0001c0002t0002g0060a0001c0002t0002g0071a0001c0002t0002g0073others(23): Show | 26 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1850-162_1850-151d others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(6): Show |
10 | a0001c0002t0002g0050a0001c0002t0002g0054a0001c0002t0002g0061others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1850-163_1850-151d others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0022g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1850-164_1850-151d others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859252
|
CTTT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1850-153_1850-151d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | ||||||
chr9:122859331
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1850-229C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859331 | ||||||
chr9:122859529
|
G | A | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1849+388C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859529 | ||||||
chr9:122859540
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1849+377C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859540 | ||||||
chr9:122859593
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1849+324G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859593 | ||||||
chr9:122859799
|
T | A | 1 | a0001c0006t0021g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1849+118A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859799 | ||||||
chr9:122860316
|
G | A | 3 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069 | 3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1635-185C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860316 | ||||||
chr9:122860368
|
G | C | 1 | a0001c0001t0017g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1635-237C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860368 | ||||||
chr9:122860369
|
A | T | 1 | a0001c0001t0017g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1635-238T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860369 | ||||||
chr9:122860405
|
CT | C | 128 | a0001c0001t0001g0228a0001c0001t0001g0240a0001c0002t0002g0004others(125): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1635-275delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860405 | ||||||
chr9:122860405
|
CTT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1635-276_1635-275d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860405 | ||||||
chr9:122860574
|
C | A | 1 | a0001c0002t0002g0112 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1635-443G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860574 | ||||||
chr9:122860703
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1635-572G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860703 | ||||||
chr9:122860915
|
A | T | 1 | a0001c0002t0002g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1635-784T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860915 | ||||||
chr9:122861176
|
G | A | 74 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(71): Show | 75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1635-1045C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861176 | ||||||
chr9:122861219
|
G | A | 2 | a0001c0002t0002g0300a0001c0002t0008g0062 | 2 | HG02451.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.1635-1088C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861219 | ||||||
chr9:122861347
|
G | A | 74 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(71): Show | 75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1635-1216C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861347 | ||||||
chr9:122861359
|
C | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1635-1228G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861359 | ||||||
chr9:122861466
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0043 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1635-1335C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861466 | ||||||
chr9:122861485
|
C | T | 1 | a0002c0003t0002g0016 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1635-1354G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861485 | ||||||
chr9:122861490
|
CA | C | 113 | a0001c0001t0001g0262a0001c0001t0019g0257a0001c0002t0002g0004others(110): Show | 114 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1635-1360delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861490 | ||||||
chr9:122861500
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0192 | 4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635-1369T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861500 | ||||||
chr9:122861505
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1635-1374T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861505 | ||||||
chr9:122861515
|
G | GA | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1635-1385dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861515 | ||||||
chr9:122861734
|
G | A | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1635-1603C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861734 | ||||||
chr9:122861735
|
T | C | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1635-1604A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861735 | ||||||
chr9:122861760
|
G | A | 1 | a0001c0002t0002g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1635-1629C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861760 | ||||||
chr9:122861844
|
A | C | 5 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0179others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635-1713T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861844 | ||||||
chr9:122861867
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0032 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1635-1736C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861867 | ||||||
chr9:122861880
|
G | C | 5 | a0001c0001t0001g0213a0001c0001t0001g0249a0001c0001t0001g0258others(2): Show | 5 | HG02698.hp2 HG03704.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1635-1749C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861880 | ||||||
chr9:122861885
|
T | C | 126 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(123): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1635-1754A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861885 | ||||||
chr9:122861968
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1635-1837A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861968 | ||||||
chr9:122862024
|
G | A | 3 | a0001c0002t0002g0138a0001c0002t0002g0140a0001c0002t0002g0145 | 3 | NA18955.hp1 NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1635-1893C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862024 | ||||||
chr9:122862120
|
A | C | 1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1635-1989T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862120 | ||||||
chr9:122862241
|
G | C | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1635-2110C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862241 | ||||||
chr9:122862297
|
T | C | 1 | a0001c0001t0003g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1635-2166A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862297 | ||||||
chr9:122862338
|
A | G | 3 | a0001c0005t0004g0090a0001c0005t0004g0120a0001c0005t0004g0121 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1635-2207T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862338 | ||||||
chr9:122862540
|
CCTGTGTT others(19): Show |
C | 3 | a0001c0002t0002g0048a0001c0002t0002g0056a0001c0002t0002g0057 | 3 | HG02970.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1635-2435_1635-241 others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862540 | ||||||
chr9:122862651
|
T | C | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-2520A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862651 | ||||||
chr9:122862702
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1635-2571G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862702 | ||||||
chr9:122862891
|
C | CA | 36 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0154others(33): Show | 37 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1634+2457dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862891 | ||||||
chr9:122863017
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0278 | 2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1634+2332T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863017 | ||||||
chr9:122863188
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1634+2161G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863188 | ||||||
chr9:122863876
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1634+1473A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863876 | ||||||
chr9:122863926
|
G | A | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1634+1423C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863926 | ||||||
chr9:122864068
|
A | G | 7 | a0001c0001t0001g0207a0001c0001t0001g0217a0001c0001t0001g0225others(4): Show | 7 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634+1281T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864068 | ||||||
chr9:122864356
|
ACACT | A | 57 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1634+989_1634+992d others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864356 | ||||||
chr9:122864370
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1634+979A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864370 | ||||||
chr9:122864617
|
G | T | 1 | a0001c0002t0002g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1634+732C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864617 | ||||||
chr9:122864621
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0245 | 2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1634+728G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864621 | ||||||
chr9:122864765
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1634+584A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864765 | ||||||
chr9:122864816
|
G | C | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634+533C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864816 | ||||||
chr9:122864892
|
GGGAT | G | 6 | a0001c0002t0002g0053a0001c0002t0002g0074a0001c0002t0002g0082others(3): Show | 6 | HG00673.hp1 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+453_1634+456d others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864892 | ||||||
chr9:122864897
|
T | C | 6 | a0001c0002t0002g0053a0001c0002t0002g0074a0001c0002t0002g0082others(3): Show | 6 | HG00673.hp1 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+452A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864897 | ||||||
chr9:122865088
|
C | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634+261G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865088 | ||||||
chr9:122865088
|
C | T | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0056others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634+261G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865088 | ||||||
chr9:122865229
|
T | A | 1 | a0001c0002t0002g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1634+120A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865229 | ||||||
chr9:122865230
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1634+119G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865230 | ||||||
chr9:122865330
|
A | G | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+19T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865330 | ||||||
chr9:122865845
|
T | TATGCCAT others(15): Show |
1 | a0001c0002t0002g0112 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1326-210_1326-189d others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865845 | ||||||
chr9:122865894
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326-237A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865894 | ||||||
chr9:122865901
|
AT | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-245delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865901 | ||||||
chr9:122866094
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1326-437A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866094 | ||||||
chr9:122866267
|
G | A | 3 | a0001c0005t0004g0090a0001c0005t0004g0120a0001c0005t0004g0121 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1326-610C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866267 | ||||||
chr9:122866360
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1326-703A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866360 | ||||||
chr9:122866360
|
T | TCTCCCC | 3 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0029g0152 | 3 | HG01891.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1326-709_1326-704d others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866360 | ||||||
chr9:122866379
|
C | CT | 3 | a0001c0001t0003g0252a0001c0002t0002g0107a0001c0005t0004g0046 | 3 | HG01175.hp2 HG01243.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | ||||||
chr9:122866379
|
C | CTCCCCCT | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1326-723_1326-722i others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | ||||||
chr9:122866379
|
C | CTCCCCCT others(17): Show |
2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | ||||||
chr9:122866379
|
C | CTCCCCCT others(17): Show |
2 | a0001c0002t0002g0141a0001c0002t0002g0182 | 2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | ||||||
chr9:122866379
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1326-722G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | ||||||
chr9:122866381
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326-724A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866381 | ||||||
chr9:122866391
|
CACG | C | 3 | a0001c0002t0002g0004a0001c0002t0002g0084a0001c0002t0002g0108 | 4 | HG01256.hp1 HG01258.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-737_1326-735d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866391 | ||||||
chr9:122866393
|
C | T | 4 | a0001c0002t0002g0048a0001c0002t0002g0056a0001c0002t0002g0057others(1): Show | 4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-736G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866393 | ||||||
chr9:122866395
|
G | C | 3 | a0001c0002t0002g0004a0001c0002t0002g0084a0001c0002t0002g0108 | 4 | HG01256.hp1 HG01258.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-738C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866395 | ||||||
chr9:122866425
|
T | C | 1 | a0001c0002t0002g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1326-768A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866425 | ||||||
chr9:122866484
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0236others(1): Show | 5 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326-827G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866484 | ||||||
chr9:122866485
|
G | GGCTCACT others(11): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0034 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1326-846_1326-829d others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866485 | ||||||
chr9:122866556
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(23): Show | 28 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.1326-899G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866556 | ||||||
chr9:122866557
|
G | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-900C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866557 | ||||||
chr9:122866559
|
C | A | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-902G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866559 | ||||||
chr9:122866562
|
G | A | 1 | a0001c0006t0015g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1326-905C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866562 | ||||||
chr9:122866604
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-947T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866604 | ||||||
chr9:122866688
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1326-1031T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866688 | ||||||
chr9:122866771
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-1114C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866771 | ||||||
chr9:122866812
|
A | C | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326-1155T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866812 | ||||||
chr9:122866857
|
T | TGGCCGCC others(608): Show |
1 | a0001c0002t0002g0143 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1326-1201_1326-120 others(619): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | ||||||
chr9:122866857
|
T | TGGCCGCC others(605): Show |
69 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(66): Show | 70 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1326-1201_1326-120 others(616): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | ||||||
chr9:122866857
|
T | TGGCCGCC others(1266): Show |
1 | a0001c0002t0002g0136 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1326-1201_1326-120 others(1277): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | ||||||
chr9:122866857
|
T | TGGCCGCC others(605): Show |
2 | a0001c0002t0002g0074a0001c0002t0002g0103 | 2 | HG00673.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1326-1201_1326-120 others(616): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | ||||||
chr9:122866861
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1326-1204G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866861 | ||||||
chr9:122866935
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1326-1278G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866935 | ||||||
chr9:122866980
|
A | G | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-1323T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866980 | ||||||
chr9:122867037
|
C | T | 1 | a0001c0006t0021g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1326-1380G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867037 | ||||||
chr9:122867055
|
A | ACCCCCGT others(607): Show |
1 | a0001c0002t0002g0066 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1326-1399_1326-139 others(618): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867055 | ||||||
chr9:122867136
|
C | T | 1 | a0002c0003t0020g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1326-1479G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867136 | ||||||
chr9:122867152
|
AG | A | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-1496delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867152 | ||||||
chr9:122867212
|
ACCCCGTC others(42): Show |
A | 37 | a0001c0002t0002g0061a0001c0002t0002g0067a0001c0002t0002g0068others(34): Show | 37 | HG00323.hp2 HG00544.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1326-1604_1326-155 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867212 | ||||||
chr9:122867212
|
ACCCCGTC others(703): Show |
A | 4 | a0001c0001t0001g0027a0001c0001t0001g0259a0001c0002t0002g0060others(1): Show | 4 | HG02135.hp2 HG02723.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2265_1326-155 others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867212 | ||||||
chr9:122867231
|
T | TGGGGGGG others(606): Show |
2 | a0001c0002t0002g0138a0001c0002t0002g0145 | 2 | NA18955.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1326-1575_1326-157 others(617): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867231 | ||||||
chr9:122867238
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1326-1581T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867238 | ||||||
chr9:122867261
|
G | GCCCCGTC others(556): Show |
1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326-1605_1326-160 others(567): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867261 | ||||||
chr9:122867269
|
C | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-1612G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867269 | ||||||
chr9:122867298
|
G | A | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-1641C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867298 | ||||||
chr9:122867319
|
G | A | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0056others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-1662C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867319 | ||||||
chr9:122867366
|
GAGACCCT others(654): Show |
G | 16 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-2370_1326-171 others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867366 | ||||||
chr9:122867369
|
A | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1326-1712T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867369 | ||||||
chr9:122867414
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0255a0001c0001t0001g0295 | 3 | NA18990.hp1 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1326-1757C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867414 | ||||||
chr9:122867509
|
GCCTCTGC others(32): Show |
G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1326-1891_1326-185 others(43): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867509 | ||||||
chr9:122867590
|
C | T | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-1933G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867590 | ||||||
chr9:122867643
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1326-1986A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867643 | ||||||
chr9:122867713
|
G | A | 77 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(74): Show | 78 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1326-2056C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867713 | ||||||
chr9:122867752
|
C | A | 1 | a0001c0006t0021g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1326-2095G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867752 | ||||||
chr9:122867768
|
GGAGGAGA others(33): Show |
G | 13 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0202others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1326-2151_1326-211 others(44): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867768 | ||||||
chr9:122867815
|
C | A | 2 | a0001c0002t0002g0100a0001c0002t0002g0114 | 2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1326-2158G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867815 | ||||||
chr9:122867825
|
C | T | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2168G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867825 | ||||||
chr9:122867847
|
G | T | 1 | a0001c0002t0002g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326-2190C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867847 | ||||||
chr9:122867873
|
ACCCCGTC others(42): Show |
A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1326-2265_1326-221 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867873 | ||||||
chr9:122867873
|
ACCCCGTC others(91): Show |
A | 11 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0187others(8): Show | 12 | HG01069.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1326-2314_1326-221 others(102): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867873 | ||||||
chr9:122867893
|
GGGGGGGT others(41): Show |
G | 2 | a0001c0001t0003g0205a0001c0001t0003g0209 | 2 | HG02056.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1326-2284_1326-223 others(52): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867893 | ||||||
chr9:122867905
|
C | CCCCCGCC others(169): Show |
3 | a0001c0001t0003g0148a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | HG01070.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1326-2249_1326-224 others(180): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867905 | ||||||
chr9:122867913
|
C | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2256G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867913 | ||||||
chr9:122867914
|
A | G | 119 | a0001c0001t0001g0281a0001c0001t0003g0148a0001c0001t0003g0291others(116): Show | 120 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1326-2257T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867914 | ||||||
chr9:122867927
|
G | A | 1 | a0001c0002t0002g0136 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1326-2270C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867927 | ||||||
chr9:122867947
|
G | T | 1 | a0003c0008t0001g0035 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1326-2290C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867947 | ||||||
chr9:122867958
|
C | G | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0056others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-2301G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867958 | ||||||
chr9:122867979
|
C | T | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2322G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867979 | ||||||
chr9:122868002
|
C | A | 1 | a0001c0001t0017g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1326-2345G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868002 | ||||||
chr9:122868027
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1326-2370T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868027 | ||||||
chr9:122868053
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-2396G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868053 | ||||||
chr9:122868123
|
T | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1326-2466A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868123 | ||||||
chr9:122868134
|
C | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-2477G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868134 | ||||||
chr9:122868134
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1326-2477G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868134 | ||||||
chr9:122868138
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1326-2481G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868138 | ||||||
chr9:122868147
|
G | A | 1 | a0001c0001t0028g0294 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1326-2490C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868147 | ||||||
chr9:122868272
|
T | C | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2615A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868272 | ||||||
chr9:122868279
|
T | G | 1 | a0001c0002t0002g0099 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1326-2622A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868279 | ||||||
chr9:122868339
|
T | A | 9 | a0001c0001t0001g0207a0001c0001t0001g0217a0001c0001t0001g0225others(6): Show | 9 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1326-2682A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868339 | ||||||
chr9:122868343
|
G | C | 1 | a0001c0002t0002g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1326-2686C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868343 | ||||||
chr9:122868391
|
G | C | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2734C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868391 | ||||||
chr9:122868482
|
C | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1326-2825G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868482 | ||||||
chr9:122868495
|
A | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1326-2838T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868495 | ||||||
chr9:122868507
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1326-2850C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868507 | ||||||
chr9:122868551
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-2894C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868551 | ||||||
chr9:122868551
|
G | C | 1 | a0002c0003t0002g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1326-2894C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868551 | ||||||
chr9:122868557
|
A | G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-2900T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868557 | ||||||
chr9:122868643
|
C | T | 1 | a0001c0001t0013g0153 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1326-2986G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868643 | ||||||
chr9:122868741
|
AAAAT | A | 30 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(27): Show | 30 | HG00438.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1326-3088_1326-308 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868741 | ||||||
chr9:122868835
|
CTATATGT others(5): Show |
C | 2 | a0001c0002t0002g0126a0001c0002t0002g0127 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1326-3190_1326-317 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868835 | ||||||
chr9:122868837
|
ATATGTGT others(5): Show |
A | 4 | a0001c0002t0002g0083a0002c0003t0002g0015a0002c0003t0002g0016others(1): Show | 4 | HG02155.hp1 NA18945.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3192_1326-318 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | ||||||
chr9:122868837
|
ATATGTGT others(7): Show |
A | 6 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069others(3): Show | 6 | NA18947.hp1 NA18971.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3194_1326-318 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | ||||||
chr9:122868837
|
ATATGTGT others(9): Show |
A | 1 | a0002c0003t0002g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1326-3196_1326-318 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | ||||||
chr9:122868837
|
ATATGTGT others(13): Show |
A | 1 | a0002c0003t0002g0014 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1326-3200_1326-318 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | ||||||
chr9:122868839
|
ATG | A | 3 | a0001c0002t0002g0053a0001c0004t0004g0122a0001c0007t0005g0045 | 3 | HG03540.hp1 HG06807.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1326-3184_1326-318 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTG | A | 5 | a0001c0002t0002g0131a0001c0002t0002g0136a0001c0002t0002g0174others(2): Show | 5 | HG01106.hp1 HG02055.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-3186_1326-318 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTG | A | 23 | a0001c0001t0005g0165a0001c0002t0002g0004a0001c0002t0002g0051others(20): Show | 24 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1326-3188_1326-318 others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(1): Show |
A | 23 | a0001c0002t0002g0075a0001c0002t0002g0080a0001c0002t0002g0085others(20): Show | 23 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1326-3190_1326-318 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(3): Show |
A | 23 | a0001c0001t0005g0011a0001c0001t0011g0149a0001c0001t0011g0150others(20): Show | 23 | HG00438.hp1 HG01109.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1326-3192_1326-318 others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(5): Show |
A | 9 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0301others(6): Show | 9 | HG00280.hp2 HG00741.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.1326-3194_1326-318 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(7): Show |
A | 6 | a0001c0001t0001g0158a0001c0001t0001g0164a0001c0002t0002g0108others(3): Show | 6 | HG00323.hp1 HG02132.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3196_1326-318 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(9): Show |
A | 18 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(15): Show | 19 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1326-3198_1326-318 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0013g0153a0001c0001t0013g0155 | 2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1326-3200_1326-318 others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1326-3202_1326-318 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(15): Show |
A | 11 | a0001c0001t0001g0208a0001c0001t0001g0228a0001c0001t0001g0230others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-3204_1326-318 others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868839
|
ATGTGTGT others(19): Show |
A | 1 | a0001c0002t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1326-3208_1326-318 others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | ||||||
chr9:122868845
|
G | A | 1 | a0001c0002t0002g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1326-3188C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868845 | ||||||
chr9:122868859
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0267others(1): Show | 4 | HG01169.hp1 HG01169.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3202C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868859 | ||||||
chr9:122868863
|
G | A | 1 | a0001c0001t0026g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1326-3206C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868863 | ||||||
chr9:122868863
|
GTGTGTGT others(26): Show |
G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0267others(1): Show | 4 | HG01169.hp1 HG01169.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3239_1326-320 others(37): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868863 | ||||||
chr9:122868867
|
G | A | 26 | a0001c0001t0001g0009a0001c0001t0001g0215a0001c0001t0001g0216others(23): Show | 27 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1326-3210C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868867 | ||||||
chr9:122868867
|
GTGTGTGT others(22): Show |
G | 1 | a0001c0001t0026g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1326-3239_1326-321 others(33): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868867 | ||||||
chr9:122868869
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1326-3212C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868869 | ||||||
chr9:122868871
|
G | A | 8 | a0001c0001t0001g0201a0001c0001t0001g0233a0001c0001t0001g0234others(5): Show | 8 | HG00099.hp2 HG01346.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-3214C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868871 | ||||||
chr9:122868871
|
GTGTGTGT others(18): Show |
G | 26 | a0001c0001t0001g0009a0001c0001t0001g0215a0001c0001t0001g0216others(23): Show | 27 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(29): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868871 | ||||||
chr9:122868873
|
GTGTGTGT others(16): Show |
G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(27): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868873 | ||||||
chr9:122868875
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0022g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1326-3234_1326-321 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868875 | ||||||
chr9:122868875
|
GTGTGTGT others(14): Show |
G | 8 | a0001c0001t0001g0201a0001c0001t0001g0233a0001c0001t0001g0234others(5): Show | 8 | HG00099.hp2 HG01346.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(25): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868875 | ||||||
chr9:122868877
|
G | A | 16 | a0001c0001t0001g0157a0001c0002t0002g0059a0001c0002t0002g0060others(13): Show | 16 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-3220C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868877 | ||||||
chr9:122868877
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0002g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1326-3234_1326-322 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868877 | ||||||
chr9:122868879
|
G | A | 2 | a0001c0002t0002g0072a0001c0002t0008g0049 | 2 | HG00733.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1326-3222C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868879 | ||||||
chr9:122868881
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1326-3224C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868881 | ||||||
chr9:122868881
|
GTGTGTGT others(8): Show |
G | 1 | a0001c0001t0001g0157 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1326-3239_1326-322 others(19): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868881 | ||||||
chr9:122868882
|
TGTGTGTG others(4): Show |
T | 15 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(12): Show | 15 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-3236_1326-322 others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868882 | ||||||
chr9:122868883
|
G | A | 1 | a0001c0001t0005g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1326-3226C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868883 | ||||||
chr9:122868893
|
G | A | 2 | a0001c0002t0002g0061a0001c0002t0022g0124 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1326-3236C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868893 | ||||||
chr9:122868912
|
TTGTG | T | 17 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(14): Show | 17 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1326-3259_1326-325 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868912 | ||||||
chr9:122868913
|
TG | T | 90 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(87): Show | 91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1326-3257delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868913 | ||||||
chr9:122868914
|
G | T | 14 | a0001c0002t0002g0061a0001c0002t0002g0085a0001c0002t0002g0097others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1326-3257C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868914 | ||||||
chr9:122868916
|
G | T | 97 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(94): Show | 98 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1326-3259C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868916 | ||||||
chr9:122868922
|
G | T | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1326-3265C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868922 | ||||||
chr9:122868945
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-3288T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868945 | ||||||
chr9:122869045
|
G | T | 3 | a0001c0005t0004g0090a0001c0005t0004g0120a0001c0005t0004g0121 | 3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1326-3388C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869045 | ||||||
chr9:122869294
|
A | G | 1 | a0001c0002t0002g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1326-3637T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869294 | ||||||
chr9:122869308
|
T | A | 2 | a0001c0002t0008g0049a0001c0002t0016g0063 | 2 | NA18957.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1326-3651A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869308 | ||||||
chr9:122869315
|
T | C | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-3658A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869315 | ||||||
chr9:122869373
|
T | C | 2 | a0001c0001t0007g0308a0001c0001t0007g0309 | 2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1326-3716A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869373 | ||||||
chr9:122869503
|
C | G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-3846G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869503 | ||||||
chr9:122869560
|
AT | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1326-3904delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | ||||||
chr9:122869560
|
ATT | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0183others(78): Show | 82 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1326-3905_1326-390 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | ||||||
chr9:122869560
|
ATTT | A | 71 | a0001c0001t0001g0034a0001c0002t0002g0004a0001c0002t0002g0050others(68): Show | 72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1326-3906_1326-390 others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | ||||||
chr9:122869560
|
ATTTT | A | 6 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(3): Show | 6 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3907_1326-390 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | ||||||
chr9:122869598
|
C | T | 4 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3941G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869598 | ||||||
chr9:122869712
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-4055G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869712 | ||||||
chr9:122869955
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-4298A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869955 | ||||||
chr9:122870044
|
A | C | 1 | a0001c0002t0002g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326-4387T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870044 | ||||||
chr9:122870056
|
G | A | 4 | a0001c0002t0002g0054a0001c0002t0002g0061a0001c0002t0022g0124others(1): Show | 4 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-4399C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870056 | ||||||
chr9:122870192
|
T | C | 1 | a0001c0006t0015g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1326-4535A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870192 | ||||||
chr9:122870366
|
C | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1326-4709G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870366 | ||||||
chr9:122870372
|
C | G | 1 | a0001c0010t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1326-4715G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870372 | ||||||
chr9:122870377
|
AAAAC | A | 3 | a0001c0001t0003g0252a0001c0001t0005g0011a0001c0001t0005g0165 | 3 | HG01952.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1326-4724_1326-472 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | ||||||
chr9:122870377
|
AAAACAAA others(1): Show |
A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1326-4728_1326-472 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | ||||||
chr9:122870377
|
AAAACAAA others(5): Show |
A | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-4732_1326-472 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | ||||||
chr9:122870377
|
AAAACAAA others(13): Show |
A | 5 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 6 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-4740_1326-472 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | ||||||
chr9:122870380
|
A | G | 2 | a0001c0002t0002g0061a0001c0002t0022g0124 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1326-4723T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870380 | ||||||
chr9:122870394
|
AAACAAAC others(12): Show |
A | 18 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(15): Show | 19 | HG00280.hp2 HG00741.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1326-4756_1326-473 others(23): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870394 | ||||||
chr9:122870395
|
AACAAACA others(11): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1326-4756_1326-473 others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870395 | ||||||
chr9:122870402
|
AAACAAAC others(4): Show |
A | 18 | a0001c0002t0002g0051a0001c0002t0002g0067a0001c0002t0002g0068others(15): Show | 18 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(15): Show |
intron_variant | MODIFIER | c.1326-4756_1326-474 others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870402 | ||||||
chr9:122870405
|
CAAACAAA others(5): Show |
C | 1 | a0001c0005t0004g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1326-4760_1326-474 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870405 | ||||||
chr9:122870406
|
AAACAAAC | A | 76 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0053others(73): Show | 77 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1326-4756_1326-475 others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870406 | ||||||
chr9:122870409
|
CAAACAAA others(1): Show |
C | 5 | a0001c0001t0001g0276a0001c0001t0011g0149a0001c0001t0011g0150others(2): Show | 5 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-4760_1326-475 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870409 | ||||||
chr9:122870410
|
AAAC | A | 12 | a0001c0001t0005g0166a0001c0002t0002g0059a0001c0002t0002g0173others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326-4756_1326-475 others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870410 | ||||||
chr9:122870413
|
C | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(24): Show | 29 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.1326-4756G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870413 | ||||||
chr9:122870647
|
T | G | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1326-4990A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870647 | ||||||
chr9:122871185
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1326-5528G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871185 | ||||||
chr9:122871359
|
G | A | 12 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069others(9): Show | 12 | HG00544.hp1 HG02155.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326-5702C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871359 | ||||||
chr9:122871387
|
T | A | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1326-5730A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871387 | ||||||
chr9:122871488
|
G | A | 1 | a0001c0002t0002g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1326-5831C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871488 | ||||||
chr9:122871506
|
T | TG | 28 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0158others(25): Show | 28 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1326-5850dupC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871506 | ||||||
chr9:122871506
|
TG | T | 73 | a0001c0001t0001g0187a0001c0002t0002g0004a0001c0002t0002g0050others(70): Show | 74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1326-5850delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871506 | ||||||
chr9:122871512
|
G | T | 13 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069others(10): Show | 13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1326-5855C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871512 | ||||||
chr9:122871545
|
G | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-5888C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871545 | ||||||
chr9:122871566
|
G | C | 1 | a0001c0002t0002g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1325+5905C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871566 | ||||||
chr9:122871627
|
G | A | 1 | a0001c0011t0002g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1325+5844C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871627 | ||||||
chr9:122871924
|
G | A | 13 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069others(10): Show | 13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+5547C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871924 | ||||||
chr9:122872329
|
T | C | 132 | a0001c0001t0001g0296a0001c0001t0011g0149a0001c0001t0011g0150others(129): Show | 133 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1325+5142A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122872329 | ||||||
chr9:122872382
|
C | A | 1 | a0001c0001t0013g0153 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1325+5089G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122872382 | ||||||
chr9:122873038
|
A | T | 16 | a0001c0001t0001g0296a0001c0004t0004g0012a0001c0004t0004g0089others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325+4433T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873038 | ||||||
chr9:122873148
|
C | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1325+4323G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873148 | ||||||
chr9:122873162
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1325+4309G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873162 | ||||||
chr9:122873326
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1325+4145T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873326 | ||||||
chr9:122873491
|
T | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0215a0001c0001t0001g0216others(26): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325+3980A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873491 | ||||||
chr9:122873847
|
T | G | 1 | a0003c0008t0001g0035 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1325+3624A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873847 | ||||||
chr9:122873943
|
G | A | 74 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(71): Show | 75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1325+3528C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873943 | ||||||
chr9:122874046
|
A | G | 3 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069 | 3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1325+3425T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874046 | ||||||
chr9:122874183
|
G | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0185others(83): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1325+3288C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874183 | ||||||
chr9:122874212
|
A | G | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1325+3259T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874212 | ||||||
chr9:122874248
|
A | G | 1 | a0002c0003t0002g0016 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1325+3223T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874248 | ||||||
chr9:122874260
|
G | C | 1 | a0001c0002t0002g0065 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1325+3211C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874260 | ||||||
chr9:122874540
|
CAG | C | 125 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(122): Show | 126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1325+2929_1325+293 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874540 | ||||||
chr9:122874586
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0001g0241 | 3 | HG01884.hp2 HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1325+2885G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874586 | ||||||
chr9:122874974
|
G | A | 1 | a0001c0002t0002g0084 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1325+2497C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874974 | ||||||
chr9:122875042
|
A | C | 2 | a0001c0002t0002g0097a0001c0002t0002g0098 | 2 | NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1325+2429T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875042 | ||||||
chr9:122875192
|
A | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1325+2279T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875192 | ||||||
chr9:122875369
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1325+2102A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875369 | ||||||
chr9:122875768
|
A | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0285a0004c0009t0001g0289 | 3 | HG00558.hp1 HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1325+1703T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875768 | ||||||
chr9:122876022
|
A | G | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+1449T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876022 | ||||||
chr9:122876111
|
T | C | 1 | a0001c0002t0002g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1325+1360A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876111 | ||||||
chr9:122876380
|
T | C | 4 | a0001c0002t0002g0048a0001c0002t0002g0056a0001c0002t0002g0057others(1): Show | 4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+1091A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876380 | ||||||
chr9:122876390
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1325+1081C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876390 | ||||||
chr9:122876555
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1325+916C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876555 | ||||||
chr9:122876627
|
C | CA | 7 | a0001c0001t0001g0207a0001c0001t0001g0217a0001c0001t0001g0225others(4): Show | 7 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+843dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876627 | ||||||
chr9:122876704
|
A | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1325+767T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876704 | ||||||
chr9:122876749
|
T | C | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+722A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876749 | ||||||
chr9:122876872
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1325+599C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876872 | ||||||
chr9:122877153
|
T | G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1325+318A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122877153 | ||||||
chr9:122877307
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1325+164G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122877307 | ||||||
chr9:122877601
|
C | A | 1 | a0001c0002t0002g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1213-18G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877601 | ||||||
chr9:122877670
|
C | T | 4 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(1): Show | 4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-87G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877670 | ||||||
chr9:122877777
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1213-194G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877777 | ||||||
chr9:122877785
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1213-202G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877785 | ||||||
chr9:122878037
|
G | C | 1 | a0001c0001t0005g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1213-454C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878037 | ||||||
chr9:122878230
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1213-647A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878230 | ||||||
chr9:122878321
|
C | T | 1 | a0001c0011t0002g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1213-738G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878321 | ||||||
chr9:122878357
|
C | A | 1 | a0001c0001t0029g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213-774G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878357 | ||||||
chr9:122878512
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1213-929G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878512 | ||||||
chr9:122878517
|
G | A | 2 | a0001c0001t0005g0168a0001c0007t0005g0045 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1213-934C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878517 | ||||||
chr9:122878562
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0255a0001c0001t0001g0295 | 3 | NA18990.hp1 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1213-979C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878562 | ||||||
chr9:122878909
|
T | C | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1212+846A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878909 | ||||||
chr9:122878921
|
G | A | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1212+834C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878921 | ||||||
chr9:122878923
|
A | AT | 79 | a0001c0001t0001g0028a0001c0002t0002g0004a0001c0002t0002g0050others(76): Show | 80 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1212+831dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878923 | ||||||
chr9:122878923
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1212+832T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878923 | ||||||
chr9:122879085
|
C | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1212+670G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879085 | ||||||
chr9:122879254
|
C | T | 2 | a0001c0001t0005g0011a0001c0001t0005g0165 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1212+501G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879254 | ||||||
chr9:122879264
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1212+491G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879264 | ||||||
chr9:122879389
|
G | C | 20 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(17): Show | 20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1212+366C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879389 | ||||||
chr9:122879440
|
A | G | 5 | a0001c0001t0001g0236a0001c0001t0003g0148a0001c0001t0003g0290others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212+315T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879440 | ||||||
chr9:122879571
|
A | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1212+184T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879571 | ||||||
chr9:122879663
|
C | T | 2 | a0001c0001t0003g0148a0001c0001t0003g0291 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1212+92G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879663 | ||||||
chr9:122880270
|
C | T | 1 | a0001c0002t0016g0063 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.961-145G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880270 | ||||||
chr9:122880321
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0192 | 4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-196A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880321 | ||||||
chr9:122880408
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.960+186C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880408 | ||||||
chr9:122881109
|
G | C | 3 | a0001c0002t0002g0085a0001c0002t0002g0111a0001c0002t0002g0112 | 3 | HG02056.hp1 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.760-315C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881109 | ||||||
chr9:122881331
|
A | G | 1 | a0001c0006t0021g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.760-537T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881331 | ||||||
chr9:122881457
|
CA | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.760-664delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881457 | ||||||
chr9:122881457
|
CAA | C | 14 | a0001c0001t0006g0270a0001c0001t0017g0214a0001c0002t0002g0173others(11): Show | 14 | HG01109.hp2 HG01433.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-665_760-664del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881457 | ||||||
chr9:122881567
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.760-773T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881567 | ||||||
chr9:122881684
|
G | A | 1 | a0001c0005t0004g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.760-890C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881684 | ||||||
chr9:122881734
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.760-940C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881734 | ||||||
chr9:122881756
|
C | T | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.760-962G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881756 | ||||||
chr9:122881822
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0193 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.760-1028C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881822 | ||||||
chr9:122881826
|
A | C | 1 | a0001c0002t0002g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.760-1032T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881826 | ||||||
chr9:122881867
|
T | C | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.760-1073A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881867 | ||||||
chr9:122882038
|
A | G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.759+1166T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882038 | ||||||
chr9:122882329
|
A | G | 1 | a0001c0002t0002g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759+875T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882329 | ||||||
chr9:122882402
|
A | C | 1 | a0001c0001t0001g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.759+802T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882402 | ||||||
chr9:122882743
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.759+461A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882743 | ||||||
chr9:122883141
|
T | C | 1 | a0001c0001t0006g0274 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.759+63A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122883141 | ||||||
chr9:122883192
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.759+12G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122883192 | ||||||
chr9:122883482
|
C | T | 1 | a0001c0002t0002g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.584-103G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883482 | ||||||
chr9:122883515
|
C | T | 1 | a0002c0003t0002g0017 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.584-136G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883515 | ||||||
chr9:122883523
|
G | T | 20 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(17): Show | 20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.584-144C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883523 | ||||||
chr9:122883548
|
C | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0266 | 2 | HG00544.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.584-169G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883548 | ||||||
chr9:122883731
|
C | T | 9 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0006g0029others(6): Show | 9 | HG00408.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.584-352G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883731 | ||||||
chr9:122884002
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.584-623G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884002 | ||||||
chr9:122884037
|
G | GT | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-659dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884037 | ||||||
chr9:122884130
|
T | C | 11 | a0001c0002t0002g0004a0001c0002t0002g0129a0001c0002t0002g0130others(8): Show | 12 | HG00621.hp1 HG01081.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.584-751A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884130 | ||||||
chr9:122884220
|
G | T | 126 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(123): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.584-841C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884220 | ||||||
chr9:122884298
|
A | T | 1 | a0001c0006t0015g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.584-919T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884298 | ||||||
chr9:122884345
|
C | T | 1 | a0001c0002t0002g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.584-966G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884345 | ||||||
chr9:122884428
|
A | T | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-1049T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884428 | ||||||
chr9:122884637
|
G | A | 2 | a0001c0002t0002g0061a0001c0002t0022g0124 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.584-1258C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884637 | ||||||
chr9:122884739
|
G | A | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.584-1360C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884739 | ||||||
chr9:122884771
|
T | C | 1 | a0001c0001t0003g0256 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.584-1392A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884771 | ||||||
chr9:122884835
|
T | C | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.584-1456A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884835 | ||||||
chr9:122885088
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.584-1709A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885088 | ||||||
chr9:122885603
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.584-2224A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885603 | ||||||
chr9:122885680
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.584-2301A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885680 | ||||||
chr9:122885867
|
TTTTTG | T | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.584-2493_584-2489d others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885867 | ||||||
chr9:122885888
|
T | A | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-2509A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885888 | ||||||
chr9:122886225
|
A | G | 125 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(122): Show | 126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.584-2846T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886225 | ||||||
chr9:122886227
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.584-2848C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886227 | ||||||
chr9:122886228
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.584-2849A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886228 | ||||||
chr9:122886241
|
T | C | 1 | a0002c0003t0002g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.584-2862A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886241 | ||||||
chr9:122886323
|
G | C | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-2944C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886323 | ||||||
chr9:122886416
|
T | C | 2 | a0001c0002t0002g0126a0001c0002t0002g0127 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.584-3037A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886416 | ||||||
chr9:122886461
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.584-3082A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886461 | ||||||
chr9:122886644
|
C | T | 3 | a0001c0002t0002g0067a0001c0002t0002g0068a0001c0002t0002g0069 | 3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.584-3265G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886644 | ||||||
chr9:122886735
|
T | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.584-3356A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886735 | ||||||
chr9:122886811
|
G | GT | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-3433dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886811 | ||||||
chr9:122886991
|
A | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG00099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+3321T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886991 | ||||||
chr9:122887102
|
C | T | 125 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(122): Show | 126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.583+3210G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887102 | ||||||
chr9:122887145
|
C | T | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+3167G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887145 | ||||||
chr9:122887211
|
T | C | 1 | a0001c0001t0007g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.583+3101A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887211 | ||||||
chr9:122887308
|
T | C | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.583+3004A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887308 | ||||||
chr9:122887319
|
G | A | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.583+2993C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887319 | ||||||
chr9:122887485
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.583+2827C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887485 | ||||||
chr9:122887570
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0185others(33): Show | 39 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.583+2742A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887570 | ||||||
chr9:122887741
|
C | CTTT | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.583+2568_583+2570d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887741 | ||||||
chr9:122887741
|
CT | C | 125 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0164others(122): Show | 126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.583+2570delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887741 | ||||||
chr9:122887789
|
G | C | 2 | a0001c0001t0013g0153a0001c0001t0013g0155 | 2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.583+2523C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887789 | ||||||
chr9:122887867
|
G | A | 1 | a0001c0001t0007g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.583+2445C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887867 | ||||||
chr9:122887967
|
A | C | 1 | a0001c0001t0001g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.583+2345T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887967 | ||||||
chr9:122888095
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0208a0001c0001t0023g0251 | 3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.583+2217T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888095 | ||||||
chr9:122888103
|
T | C | 1 | a0002c0003t0002g0021 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.583+2209A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888103 | ||||||
chr9:122888117
|
T | G | 1 | a0001c0001t0001g0003 | 2 | HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.583+2195A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888117 | ||||||
chr9:122888169
|
A | G | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+2143T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888169 | ||||||
chr9:122888239
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0003g0040 | 4 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+2073C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888239 | ||||||
chr9:122888355
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.583+1957T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888355 | ||||||
chr9:122888734
|
C | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.583+1578G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888734 | ||||||
chr9:122888855
|
C | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.583+1457G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888855 | ||||||
chr9:122888922
|
AC | A | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+1389delG | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888922 | ||||||
chr9:122889085
|
T | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0184others(27): Show | 31 | HG01069.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.583+1227A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889085 | ||||||
chr9:122889183
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.583+1129T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889183 | ||||||
chr9:122889427
|
A | G | 1 | a0001c0001t0009g0198 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.583+885T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889427 | ||||||
chr9:122889528
|
C | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+784G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889528 | ||||||
chr9:122889636
|
G | C | 3 | a0001c0002t0002g0048a0001c0002t0002g0056a0001c0002t0002g0057 | 3 | HG02970.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.583+676C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889636 | ||||||
chr9:122889917
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.583+395T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889917 | ||||||
chr9:122890097
|
C | T | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+215G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890097 | ||||||
chr9:122890117
|
G | C | 1 | a0001c0004t0004g0122 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.583+195C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890117 | ||||||
chr9:122890150
|
A | G | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.583+162T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890150 | ||||||
chr9:122890230
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.583+82G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890230 | ||||||
chr9:122890723
|
CT | C | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.350-179delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122890723 | ||||||
chr9:122890787
|
A | G | 1 | a0001c0002t0002g0065 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.350-242T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122890787 | ||||||
chr9:122891012
|
AT | A | 124 | a0001c0001t0001g0024a0001c0001t0001g0187a0001c0001t0001g0188others(121): Show | 125 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.350-468delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | ||||||
chr9:122891012
|
ATT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.350-469_350-468del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | ||||||
chr9:122891012
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0160 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.350-478_350-468del others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | ||||||
chr9:122891012
|
ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(11): Show | 15 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.350-479_350-468del others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | ||||||
chr9:122891073
|
G | A | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-528C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891073 | ||||||
chr9:122891186
|
A | AT | 15 | a0001c0004t0004g0012a0001c0004t0004g0089a0001c0004t0004g0115others(12): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-642dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891186 | ||||||
chr9:122891267
|
C | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.350-722G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891267 | ||||||
chr9:122891270
|
G | A | 1 | a0001c0001t0028g0294 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-725C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891270 | ||||||
chr9:122891305
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.350-760C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891305 | ||||||
chr9:122891366
|
G | C | 128 | a0001c0001t0001g0288a0001c0002t0002g0004a0001c0002t0002g0048others(125): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.350-821C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891366 | ||||||
chr9:122891396
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.350-851A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891396 | ||||||
chr9:122891711
|
G | A | 1 | a0001c0002t0002g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.350-1166C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891711 | ||||||
chr9:122891811
|
A | G | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.349+1098T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891811 | ||||||
chr9:122891827
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.349+1082T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891827 | ||||||
chr9:122891861
|
TCA | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1046_349+1047d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891861 | ||||||
chr9:122892056
|
C | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+853G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892056 | ||||||
chr9:122892113
|
A | AT | 7 | a0001c0001t0001g0159a0001c0001t0001g0184a0001c0001t0001g0215others(4): Show | 7 | HG02145.hp1 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+795dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892113 | ||||||
chr9:122892373
|
A | G | 4 | a0001c0001t0001g0147a0001c0001t0010g0196a0001c0001t0010g0197others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+536T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892373 | ||||||
chr9:122892395
|
G | A | 1 | a0001c0001t0017g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.349+514C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892395 | ||||||
chr9:122892480
|
C | T | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.349+429G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892480 | ||||||
chr9:122892513
|
G | A | 10 | a0001c0002t0002g0173a0001c0002t0002g0174a0001c0002t0002g0175others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+396C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892513 | ||||||
chr9:122892702
|
C | T | 1 | a0001c0002t0002g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349+207G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892702 | ||||||
chr9:122893137
|
A | G | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.232-111T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893137 | ||||||
chr9:122893752
|
T | C | 1 | a0001c0002t0002g0072 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.232-726A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893752 | ||||||
chr9:122893767
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.232-741A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893767 | ||||||
chr9:122893768
|
C | T | 1 | a0001c0001t0017g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.232-742G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893768 | ||||||
chr9:122893989
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.232-963C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893989 | ||||||
chr9:122894076
|
G | A | 57 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.232-1050C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894076 | ||||||
chr9:122894115
|
C | T | 1 | a0001c0001t0001g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.232-1089G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894115 | ||||||
chr9:122894153
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0249 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.232-1127T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894153 | ||||||
chr9:122894176
|
G | A | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.232-1150C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894176 | ||||||
chr9:122894248
|
G | A | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.232-1222C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894248 | ||||||
chr9:122894258
|
C | CA | 15 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.232-1233dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894258 | ||||||
chr9:122894391
|
G | A | 3 | a0001c0002t0002g0085a0001c0002t0002g0111a0001c0002t0002g0112 | 3 | HG02056.hp1 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.232-1365C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894391 | ||||||
chr9:122894397
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.232-1371T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894397 | ||||||
chr9:122894508
|
T | C | 6 | a0001c0002t0002g0054a0001c0002t0002g0061a0001c0002t0002g0107others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1482A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894508 | ||||||
chr9:122894656
|
G | A | 1 | a0001c0001t0003g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232-1630C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894656 | ||||||
chr9:122894803
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232-1777G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894803 | ||||||
chr9:122894820
|
C | T | 128 | a0001c0001t0001g0296a0001c0002t0002g0004a0001c0002t0002g0048others(125): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.232-1794G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894820 | ||||||
chr9:122894903
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.232-1877A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894903 | ||||||
chr9:122895160
|
G | GT | 12 | a0001c0001t0001g0185a0001c0001t0001g0213a0001c0001t0001g0244others(9): Show | 12 | HG00639.hp1 HG01496.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+2118dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895160 | ||||||
chr9:122895160
|
GT | G | 14 | a0001c0001t0001g0164a0001c0001t0011g0149a0001c0001t0011g0150others(11): Show | 14 | HG00323.hp1 HG00544.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+2118delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895160 | ||||||
chr9:122895326
|
C | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+1953G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895326 | ||||||
chr9:122895383
|
GTCTCGAA others(1): Show |
G | 57 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.231+1888_231+1895d others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895383 | ||||||
chr9:122895388
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.231+1891C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895388 | ||||||
chr9:122895995
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(299): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.231+1284G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895995 | ||||||
chr9:122896072
|
T | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1207A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896072 | ||||||
chr9:122896073
|
C | G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1206G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896073 | ||||||
chr9:122896076
|
G | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1203C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896076 | ||||||
chr9:122896077
|
GGCCACAC others(3): Show |
G | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1192_231+1201d others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896077 | ||||||
chr9:122896088
|
A | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1191T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896088 | ||||||
chr9:122896090
|
A | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1189T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896090 | ||||||
chr9:122896098
|
A | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0123 | 2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1181T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896098 | ||||||
chr9:122896120
|
TAA | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.231+1157_231+1158d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896120 | ||||||
chr9:122896120
|
TAAA | T | 104 | a0001c0001t0001g0248a0001c0002t0002g0004a0001c0002t0002g0048others(101): Show | 105 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.231+1156_231+1158d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896120 | ||||||
chr9:122896136
|
AAAC | A | 20 | a0001c0002t0002g0059a0001c0002t0002g0060a0001c0002t0002g0065others(17): Show | 20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.231+1140_231+1142d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896136 | ||||||
chr9:122896335
|
A | G | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0056others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+944T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896335 | ||||||
chr9:122896459
|
C | T | 1 | a0001c0002t0018g0086 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.231+820G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896459 | ||||||
chr9:122896567
|
C | T | 2 | a0001c0002t0002g0080a0001c0002t0002g0104 | 2 | NA20300.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.231+712G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896567 | ||||||
chr9:122896733
|
C | CATAAGAT others(1): Show |
3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.231+538_231+545dup others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896733 | ||||||
chr9:122896770
|
C | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+509G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896770 | ||||||
chr9:122896778
|
CCTGGGAG others(5): Show |
C | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.231+489_231+500del others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896778 | ||||||
chr9:122896840
|
T | C | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.231+439A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896840 | ||||||
chr9:122896907
|
T | C | 127 | a0001c0002t0002g0004a0001c0002t0002g0048a0001c0002t0002g0050others(124): Show | 128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.231+372A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896907 | ||||||
chr9:122896924
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+355C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896924 | ||||||
chr9:122896969
|
T | C | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.231+310A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896969 | ||||||
chr9:122897024
|
T | TA | 63 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0024others(60): Show | 65 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.231+254dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | ||||||
chr9:122897024
|
T | TAA | 9 | a0001c0001t0001g0189a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+253_231+254dup others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | ||||||
chr9:122897024
|
TA | T | 24 | a0001c0001t0001g0030a0001c0001t0001g0245a0001c0001t0003g0205others(21): Show | 24 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+254delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | ||||||
chr9:122897024
|
TAA | T | 105 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(102): Show | 107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+253_231+254del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | ||||||
chr9:122897024
|
TAAA | T | 28 | a0001c0001t0007g0309a0001c0001t0011g0149a0001c0001t0011g0150others(25): Show | 28 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.231+252_231+254del others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | ||||||
chr9:122897026
|
A | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.231+253T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897026 | ||||||
chr9:122897097
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+182T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897097 | ||||||
chr9:122897241
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.231+38A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897241 | ||||||
chr9:122897790
|
A | G | 128 | a0001c0001t0001g0296a0001c0002t0002g0004a0001c0002t0002g0048others(125): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-67-214T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122897790 | ||||||
chr9:122897888
|
C | T | 1 | a0001c0002t0002g0136 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-67-312G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122897888 | ||||||
chr9:122898104
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67-528G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898104 | ||||||
chr9:122898111
|
A | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-535T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898111 | ||||||
chr9:122898157
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-67-581A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898157 | ||||||
chr9:122898165
|
G | A | 2 | a0001c0002t0002g0061a0001c0002t0022g0124 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-67-589C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898165 | ||||||
chr9:122898252
|
T | G | 1 | a0001c0001t0007g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-67-676A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898252 | ||||||
chr9:122898253
|
C | G | 78 | a0001c0002t0002g0004a0001c0002t0002g0050a0001c0002t0002g0051others(75): Show | 79 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-67-677G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898253 | ||||||
chr9:122898435
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-67-859C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898435 | ||||||
chr9:122898514
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-67-938G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898514 | ||||||
chr9:122898691
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0185others(79): Show | 87 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-67-1115C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898691 | ||||||
chr9:122898706
|
G | A | 26 | a0001c0002t0002g0004a0001c0002t0002g0051a0001c0002t0002g0083others(23): Show | 27 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-67-1130C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898706 | ||||||
chr9:122898737
|
G | A | 2 | a0001c0002t0002g0113a0001c0012t0002g0093 | 2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-67-1161C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898737 | ||||||
chr9:122898749
|
C | CA | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-67-1174dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | ||||||
chr9:122898749
|
C | CAA | 127 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0282others(124): Show | 127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-67-1175_-67-1174d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | ||||||
chr9:122898749
|
C | CAAA | 8 | a0001c0002t0002g0004a0001c0002t0002g0114a0001c0002t0002g0136others(5): Show | 9 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67-1176_-67-1174d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | ||||||
chr9:122898775
|
G | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-67-1199C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898775 | ||||||
chr9:122898780
|
G | C | 1 | a0001c0001t0001g0230 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-67-1204C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898780 | ||||||
chr9:122898877
|
G | C | 2 | a0001c0001t0007g0308a0001c0001t0007g0309 | 2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-67-1301C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898877 | ||||||
chr9:122898979
|
C | A | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.-67-1403G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898979 | ||||||
chr9:122899000
|
A | C | 1 | a0001c0002t0008g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-67-1424T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899000 | ||||||
chr9:122899004
|
T | C | 16 | a0001c0001t0001g0296a0001c0004t0004g0012a0001c0004t0004g0089others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-67-1428A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899004 | ||||||
chr9:122899090
|
GT | G | 99 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-67-1515delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | ||||||
chr9:122899090
|
GTT | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.-67-1516_-67-1515d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | ||||||
chr9:122899090
|
GTTT | G | 18 | a0001c0001t0001g0156a0001c0002t0002g0048a0001c0002t0002g0056others(15): Show | 18 | HG02109.hp1 HG02155.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67-1517_-67-1515d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | ||||||
chr9:122899090
|
GTTTTT | G | 14 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-67-1519_-67-1515d others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | ||||||
chr9:122899091
|
T | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0195 | 2 | HG01258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-67-1515A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899091 | ||||||
chr9:122899092
|
T | G | 51 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(48): Show | 51 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.-67-1516A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899092 | ||||||
chr9:122899093
|
T | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.-67-1517A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899093 | ||||||
chr9:122899118
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-67-1542A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899118 | ||||||
chr9:122899223
|
C | G | 1 | a0001c0002t0002g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-67-1647G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899223 | ||||||
chr9:122899285
|
T | C | 1 | a0001c0002t0002g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-67-1709A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899285 | ||||||
chr9:122900007
|
C | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-67-2431G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900007 | ||||||
chr9:122900116
|
T | C | 1 | a0001c0002t0002g0146 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-67-2540A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900116 | ||||||
chr9:122900212
|
T | C | 3 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-67-2636A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900212 | ||||||
chr9:122900240
|
T | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-67-2664A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900240 | ||||||
chr9:122900322
|
C | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-67-2746G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900322 | ||||||
chr9:122900342
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67-2766C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900342 | ||||||
chr9:122900437
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-67-2861A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900437 | ||||||
chr9:122900887
|
T | C | 1 | a0004c0009t0001g0289 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-67-3311A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900887 | ||||||
chr9:122900901
|
G | A | 4 | a0001c0001t0003g0148a0001c0001t0003g0290a0001c0001t0003g0291others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67-3325C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900901 | ||||||
chr9:122901174
|
T | C | 1 | a0001c0002t0002g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67-3598A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901174 | ||||||
chr9:122901194
|
A | G | 9 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(6): Show | 9 | HG00544.hp1 HG02155.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.-67-3618T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901194 | ||||||
chr9:122901263
|
T | A | 5 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0179others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-3687A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901263 | ||||||
chr9:122901460
|
A | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0154a0001c0001t0001g0156others(16): Show | 20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-68+3650T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901460 | ||||||
chr9:122901503
|
A | G | 6 | a0001c0002t0002g0048a0001c0002t0002g0054a0001c0002t0002g0056others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+3607T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901503 | ||||||
chr9:122901546
|
C | G | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+3564G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901546 | ||||||
chr9:122901576
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0187others(8): Show | 12 | HG01069.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-68+3534G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901576 | ||||||
chr9:122901586
|
CT | C | 125 | a0001c0001t0001g0293a0001c0001t0001g0295a0001c0001t0007g0309others(122): Show | 126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-68+3523delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901586 | ||||||
chr9:122901684
|
C | T | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+3426G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901684 | ||||||
chr9:122901928
|
C | CT | 10 | a0001c0001t0001g0023a0001c0001t0001g0183a0001c0001t0001g0184others(7): Show | 10 | HG00544.hp2 HG01071.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+3181dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901928 | ||||||
chr9:122902023
|
G | A | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+3087C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902023 | ||||||
chr9:122902053
|
C | T | 4 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0011g0151others(1): Show | 4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+3057G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902053 | ||||||
chr9:122902244
|
A | C | 2 | a0001c0005t0004g0046a0001c0005t0004g0047 | 2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-68+2866T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902244 | ||||||
chr9:122902252
|
T | A | 20 | a0001c0002t0002g0004a0001c0002t0002g0129a0001c0002t0002g0130others(17): Show | 21 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-68+2858A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902252 | ||||||
chr9:122902471
|
C | T | 10 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(7): Show | 10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+2639G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902471 | ||||||
chr9:122902490
|
T | C | 128 | a0001c0001t0001g0296a0001c0002t0002g0004a0001c0002t0002g0048others(125): Show | 129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-68+2620A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902490 | ||||||
chr9:122902516
|
G | A | 1 | a0001c0002t0002g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-68+2594C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902516 | ||||||
chr9:122902577
|
GCTCACGC others(7): Show |
G | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+2519_-68+2532d others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902577 | ||||||
chr9:122902593
|
C | G | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+2517G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902593 | ||||||
chr9:122902603
|
G | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-68+2507C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902603 | ||||||
chr9:122902848
|
CA | C | 117 | a0001c0001t0001g0147a0001c0001t0003g0148a0001c0002t0002g0004others(114): Show | 118 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-68+2261delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902848 | ||||||
chr9:122903109
|
TTAAATTA | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(23): Show | 28 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.-68+1994_-68+2000d others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903109 | ||||||
chr9:122903597
|
T | C | 1 | a0001c0004t0004g0297 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-68+1513A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903597 | ||||||
chr9:122903876
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-68+1234T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903876 | ||||||
chr9:122903879
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-68+1231A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903879 | ||||||
chr9:122903917
|
T | C | 2 | a0001c0006t0015g0010a0001c0006t0021g0299 | 2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+1193A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903917 | ||||||
chr9:122903980
|
C | T | 10 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(7): Show | 10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+1130G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903980 | ||||||
chr9:122904130
|
T | C | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-68+980A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904130 | ||||||
chr9:122904536
|
C | G | 1 | a0001c0004t0004g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-68+574G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904536 | ||||||
chr9:122904819
|
C | T | 1 | a0001c0001t0005g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-68+291G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904819 | ||||||
chr9:122904850
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-68+260C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904850 | ||||||
chr9:122905067
|
C | A | 1 | a0001c0001t0003g0302 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-68+43G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122905067 |